Item | Value |
---|---|
geneid | 5925 |
ensemblid | ENSG00000139687.16 |
hgncid | 9884 |
symbol | RB1 |
name | RB transcriptional corepressor 1 |
refseq_nuc | NM_000321.3 |
refseq_prot | NP_000312.2 |
ensembl_nuc | ENST00000267163.6 |
ensembl_prot | ENSP00000267163.4 |
mane_status | MANE Select |
chr | chr13 |
start | 48303751 |
end | 48481890 |
strand | + |
ver | v1.2 |
region | chr13:48303751-48481890 |
region5000 | chr13:48298751-48486890 |
regionname0 | RB1_chr13_48303751_48481890 |
regionname5000 | RB1_chr13_48298751_48486890 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 928 | 298 | 84 | 50 | 130 | 6 | 26 | 108 | RB1_chr13_48298751_48486890 | RB1 | MPPKT others(923): Show |
chr13 | 48298751 | 48486890 |
a0002 | 0/0 | 925 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | MPPKT others(920): Show |
chr13 | 48298751 | 48486890 |
a0003 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | MPPKT others(923): Show |
chr13 | 48298751 | 48486890 |
a0004 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | MPPKT others(923): Show |
chr13 | 48298751 | 48486890 |
a0005 | 0/0 | 928 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | MPPKT others(923): Show |
chr13 | 48298751 | 48486890 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2784 | 296 | 83 | 50 | 129 | 6 | 26 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 | ||
a0001c0004 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 | ||
a0001c0007 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 | ||
a0002c0002 | 0/0 | 2775 | 4 | 4 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2770): Show |
chr13 | 48298751 | 48486890 | ||
a0003c0003 | 0/0 | 2784 | 2 | 2 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 | ||
a0004c0006 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 | ||
a0005c0005 | 0/0 | 2784 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | ATGCC others(2779): Show |
chr13 | 48298751 | 48486890 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4768 | 275 | 67 | 47 | 127 | 6 | 26 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0002 | 0/0 | 4768 | 5 | 4 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0003 | 0/0 | 4768 | 4 | 3 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0004 | 0/0 | 4768 | 4 | 3 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0005 | 0/0 | 4768 | 4 | 4 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0006 | 0/0 | 4768 | 2 | 0 | 0 | 2 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0007 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0001t0008 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0004t0001 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0001c0007t0001 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0002c0002t0001 | 0/0 | 4759 | 4 | 4 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4754): Show |
chr13 | 48298751 | 48486890 |
a0003c0003t0001 | 0/0 | 4768 | 2 | 2 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0004c0006t0001 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
a0005c0005t0001 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | AGTTG others(4763): Show |
chr13 | 48298751 | 48486890 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0003g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0006g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0001c0007t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0003c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0004c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
a0005c0005t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01074 | hp2 | a0004 | c0006 | t0001 | g0173 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01109 | hp1 | a0005 | c0005 | t0001 | g0294 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | CDX | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CDX | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0210 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0253 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0274 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0211 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03516 | hp1 | a0001 | c0007 | t0001 | g0207 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0251 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18998 | hp2 | a0001 | c0001 | t0006 | g0286 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19086 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19089 | hp2 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | YRI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ASW | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | GIH | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0153 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0292 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | USA | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | USA | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | USA | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0295 | REF | REF | RB1_chr13_48298751_48486890 | RB1 | chr13 | 48298751 | 48486890 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48303948 | CGCCGCCG others(2): Show |
C | 1 | a0002 | 4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.45_53delTGCCGCCGC | p.Ala16_Ala18del | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/27 | 207/4768 | 45/2787 | 15/928 | INFO_REALIGN_3_PRIME | chr13 | 48303948 | ||
chr13:48381322 | C | G | 1 | a0003 | 2 | HG02630.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.1574C>G | p.Ala525Gly | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/27 | 1736/4768 | 1574/2787 | 525/928 | chr13 | 48381322 | |||
chr13:48465271 | C | T | 1 | a0004 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2392C>T | p.Arg798Trp | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/27 | 2554/4768 | 2392/2787 | 798/928 | chr13 | 48465271 | |||
chr13:48476746 | G | A | 1 | a0005 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2566G>A | p.Asp856Asn | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 25/27 | 2728/4768 | 2566/2787 | 856/928 | chr13 | 48476746 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48379617 | G | A | 1 | a0001c0004 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1356G>A | p.Leu452Leu | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/27 | 1518/4768 | 1356/2787 | 452/928 | chr13 | 48379617 | |||
chr13:48381380 | A | G | 1 | a0001c0007 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1632A>G | p.Arg544Arg | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/27 | 1794/4768 | 1632/2787 | 544/928 | chr13 | 48381380 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48480198 | A | G | 1 | a0001c0001t0006 | 2 | NA18998.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*127A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 127 | chr13 | 48480198 | ||||||
chr13:48480255 | A | T | 1 | a0001c0001t0005 | 4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*184A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 184 | chr13 | 48480255 | ||||||
chr13:48480534 | T | A | 1 | a0001c0001t0003 | 4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*463T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 463 | chr13 | 48480534 | ||||||
chr13:48480774 | G | T | 1 | a0001c0001t0008 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 703 | chr13 | 48480774 | ||||||
chr13:48480926 | G | A | 1 | a0001c0001t0004 | 4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 855 | chr13 | 48480926 | ||||||
chr13:48480995 | A | G | 1 | a0001c0001t0007 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*924A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 924 | chr13 | 48480995 | ||||||
chr13:48481035 | C | G | 1 | a0001c0001t0002 | 5 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*964C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 964 | chr13 | 48481035 | ||||||
chr13:48481758 | T | C | 1 | a0001c0001t0002 | 5 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1687T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 27/27 | 1687 | chr13 | 48481758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:48304135 | T | C | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.137+86T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304135 | |||||||
chr13:48304143 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+94C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304143 | |||||||
chr13:48304156 | G | A | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
111 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.137+107G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304156 | |||||||
chr13:48304239 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.137+190C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304239 | |||||||
chr13:48304555 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.137+506G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304555 | |||||||
chr13:48304711 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.137+662A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304711 | |||||||
chr13:48304742 | A | C | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | NA18998.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.137+693A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304742 | |||||||
chr13:48304864 | A | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+815A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304864 | |||||||
chr13:48304865 | TCTTGG | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+817_137+821del others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304865 | |||||||
chr13:48304873 | T | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+824T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304873 | |||||||
chr13:48304874 | C | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.137+825C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48304874 | |||||||
chr13:48305163 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+1114A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305163 | |||||||
chr13:48305263 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.137+1214G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305263 | |||||||
chr13:48305549 | A | G | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1500A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305549 | |||||||
chr13:48305600 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.137+1551C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305600 | |||||||
chr13:48305645 | TA | T | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+1602delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr13 | 48305645 | ||||||
chr13:48305769 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.138-1511G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305769 | |||||||
chr13:48305799 | G | T | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.138-1481G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305799 | |||||||
chr13:48305807 | A | T | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.138-1473A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305807 | |||||||
chr13:48305961 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.138-1319A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48305961 | |||||||
chr13:48306006 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.138-1274G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306006 | |||||||
chr13:48306126 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.138-1154C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306126 | |||||||
chr13:48306421 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.138-859A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306421 | |||||||
chr13:48306434 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.138-846A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306434 | |||||||
chr13:48306505 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.138-775C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306505 | |||||||
chr13:48306510 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.138-770A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306510 | |||||||
chr13:48306581 | T | A | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.138-699T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306581 | |||||||
chr13:48306623 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.138-657C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306623 | |||||||
chr13:48306819 | G | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.138-461G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306819 | |||||||
chr13:48306862 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-418T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306862 | |||||||
chr13:48306991 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0285 |
2 | HG00323.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.138-289A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48306991 | |||||||
chr13:48307018 | G | C | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
111 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.138-262G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48307018 | |||||||
chr13:48307060 | T | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-220T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48307060 | |||||||
chr13:48307065 | C | T | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.138-215C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48307065 | |||||||
chr13:48307109 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.138-171A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 1/26 | chr13 | 48307109 | |||||||
chr13:48307481 | T | C | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+75T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307481 | |||||||
chr13:48307573 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | NA18952.hp2 NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.264+167G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307573 | |||||||
chr13:48307582 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264+176C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307582 | |||||||
chr13:48307689 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+283T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307689 | |||||||
chr13:48307699 | C | CA | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
254 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.264+310dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48307699 | ||||||
chr13:48307699 | C | CAA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(9): Show |
12 | HG00741.hp1 HG01975.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+309_264+310dup others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48307699 | ||||||
chr13:48307843 | C | T | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+437C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307843 | |||||||
chr13:48307888 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+482T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307888 | |||||||
chr13:48307936 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+530A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48307936 | |||||||
chr13:48308050 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.264+644A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308050 | |||||||
chr13:48308180 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+774G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308180 | |||||||
chr13:48308189 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+783T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308189 | |||||||
chr13:48308206 | C | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
111 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.264+800C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308206 | |||||||
chr13:48308227 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
102 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.264+821A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308227 | |||||||
chr13:48308355 | A | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+949A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308355 | |||||||
chr13:48308369 | T | G | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264+963T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308369 | |||||||
chr13:48308651 | CA | C | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+1255delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48308651 | ||||||
chr13:48308657 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.264+1251A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308657 | |||||||
chr13:48308671 | C | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.264+1265C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308671 | |||||||
chr13:48308695 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(51): Show |
55 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.264+1289A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308695 | |||||||
chr13:48308879 | C | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+1473C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308879 | |||||||
chr13:48308939 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.264+1533A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308939 | |||||||
chr13:48308952 | A | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+1546A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48308952 | |||||||
chr13:48309216 | ACT | A | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0003g0004 others(2): Show |
6 | HG00099.hp1 HG01192.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+1813_264+1814d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48309216 | ||||||
chr13:48309235 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.264+1829A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309235 | |||||||
chr13:48309357 | G | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1951G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309357 | |||||||
chr13:48309454 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.264+2048T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309454 | |||||||
chr13:48309506 | A | C | 1 | a0001c0001t0001g0283 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.264+2100A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309506 | |||||||
chr13:48309628 | A | G | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+2222A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309628 | |||||||
chr13:48309772 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+2366G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309772 | |||||||
chr13:48309774 | T | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.264+2368T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309774 | |||||||
chr13:48309967 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+2561A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48309967 | |||||||
chr13:48310170 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.264+2764G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48310170 | |||||||
chr13:48310498 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+3092G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48310498 | |||||||
chr13:48310643 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+3237T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48310643 | |||||||
chr13:48310874 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.264+3468T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48310874 | |||||||
chr13:48311080 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+3674G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311080 | |||||||
chr13:48311135 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.264+3729T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311135 | |||||||
chr13:48311287 | A | G | 2 | a0001c0001t0001g0203 a0001c0007t0001g0207 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264+3881A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311287 | |||||||
chr13:48311460 | G | C | 17 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.264+4054G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311460 | |||||||
chr13:48311543 | A | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0282 |
3 | HG02129.hp1 NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.264+4137A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311543 | |||||||
chr13:48311587 | TCATC | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.264+4185_264+4188d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48311587 | ||||||
chr13:48311674 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+4268T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311674 | |||||||
chr13:48311675 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.264+4269C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311675 | |||||||
chr13:48311733 | G | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01074.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.264+4327G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311733 | |||||||
chr13:48311746 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+4340A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311746 | |||||||
chr13:48311819 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+4413T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311819 | |||||||
chr13:48311854 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.264+4448C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311854 | |||||||
chr13:48311894 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+4488C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311894 | |||||||
chr13:48311926 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+4520G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48311926 | |||||||
chr13:48312002 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.264+4596T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312002 | |||||||
chr13:48312146 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.264+4740G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312146 | |||||||
chr13:48312373 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+4967G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312373 | |||||||
chr13:48312587 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.264+5181A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312587 | |||||||
chr13:48312633 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG00738.hp2 HG01168.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.264+5227C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312633 | |||||||
chr13:48312671 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.264+5265G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312671 | |||||||
chr13:48312706 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.264+5300G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312706 | |||||||
chr13:48312736 | C | CT | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+5335dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48312736 | ||||||
chr13:48312886 | T | A | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.264+5480T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312886 | |||||||
chr13:48312905 | A | C | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+5499A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312905 | |||||||
chr13:48312977 | T | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0003c0003t0001g0210 others(1): Show |
4 | HG02630.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+5571T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48312977 | |||||||
chr13:48313066 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.264+5660C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313066 | |||||||
chr13:48313336 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.264+5930G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313336 | |||||||
chr13:48313363 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.264+5957G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313363 | |||||||
chr13:48313370 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
88 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.264+5974dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313370 | ||||||
chr13:48313370 | A | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG02486.hp1 HG02723.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+5964A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313370 | |||||||
chr13:48313381 | G | T | 1 | a0001c0001t0001g0296 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.264+5975G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313381 | |||||||
chr13:48313507 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+6101C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313507 | |||||||
chr13:48313526 | G | GT | 14 | a0001c0001t0001g0080 a0001c0001t0001g0125 a0001c0001t0001g0126 others(11): Show |
14 | HG02145.hp2 HG02486.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+6132dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313526 | ||||||
chr13:48313634 | A | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.264+6228A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313634 | |||||||
chr13:48313745 | C | CT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(38): Show |
42 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.264+6360dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313745 | ||||||
chr13:48313745 | C | CTT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
186 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.264+6359_264+6360d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313745 | ||||||
chr13:48313745 | C | CTTT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0075 others(10): Show |
13 | HG01952.hp2 HG02055.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.264+6358_264+6360d others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313745 | ||||||
chr13:48313745 | CT | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG00738.hp2 HG02486.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+6360delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48313745 | ||||||
chr13:48313905 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.264+6499C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313905 | |||||||
chr13:48313939 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.264+6533C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313939 | |||||||
chr13:48313985 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.264+6579G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48313985 | |||||||
chr13:48314035 | A | C | 5 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+6629A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314035 | |||||||
chr13:48314119 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+6713T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314119 | |||||||
chr13:48314221 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.264+6815A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314221 | |||||||
chr13:48314528 | G | A | 80 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(77): Show |
82 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.264+7122G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314528 | |||||||
chr13:48314644 | A | G | 17 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(14): Show |
18 | HG01192.hp2 HG02055.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.264+7238A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314644 | |||||||
chr13:48314749 | C | T | 49 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(46): Show |
50 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.264+7343C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314749 | |||||||
chr13:48314755 | C | T | 1 | a0001c0004t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.264+7349C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314755 | |||||||
chr13:48314779 | C | CA | 102 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(99): Show |
102 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.264+7384dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48314779 | ||||||
chr13:48314810 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.264+7404A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314810 | |||||||
chr13:48314913 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.264+7507C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314913 | |||||||
chr13:48314988 | A | G | 1 | a0001c0001t0001g0021 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.264+7582A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48314988 | |||||||
chr13:48315003 | A | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0086 a0001c0001t0001g0087 others(11): Show |
14 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+7597A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315003 | |||||||
chr13:48315065 | C | T | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.264+7659C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315065 | |||||||
chr13:48315288 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.264+7882T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315288 | |||||||
chr13:48315391 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.264+7985A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315391 | |||||||
chr13:48315430 | CTA | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+8026_264+8027d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48315430 | ||||||
chr13:48315444 | A | G | 7 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 others(4): Show |
8 | HG01192.hp2 HG02055.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.264+8038A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315444 | |||||||
chr13:48315674 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.264+8268T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315674 | |||||||
chr13:48315758 | C | T | 1 | a0001c0001t0003g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.264+8352C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315758 | |||||||
chr13:48315804 | TA | T | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+8401delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48315804 | ||||||
chr13:48315921 | C | G | 1 | a0001c0001t0004g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.264+8515C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315921 | |||||||
chr13:48315921 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.264+8515C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48315921 | |||||||
chr13:48316216 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+8810A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316216 | |||||||
chr13:48316323 | CGGACACT others(3): Show |
C | 11 | a0001c0001t0001g0134 a0001c0001t0001g0180 a0001c0001t0001g0181 others(8): Show |
11 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+8920_264+8929d others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316323 | ||||||
chr13:48316719 | TCA | T | 6 | a0001c0001t0001g0026 a0001c0001t0001g0133 a0001c0001t0001g0213 others(3): Show |
6 | HG00642.hp1 HG00738.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+9377_264+9378d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACA | T | 11 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(8): Show |
11 | HG00642.hp2 HG01168.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+9375_264+9378d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACA | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0105 others(10): Show |
13 | HG01069.hp2 HG01243.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+9373_264+9378d others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(1): Show |
T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
18 | HG00323.hp1 HG00558.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.264+9371_264+9378d others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(3): Show |
T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0033 others(20): Show |
23 | HG00733.hp1 HG01071.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.264+9369_264+9378d others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(5): Show |
T | 27 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(24): Show |
27 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.264+9367_264+9378d others(14): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(7): Show |
T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0024 others(25): Show |
31 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.264+9365_264+9378d others(16): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(9): Show |
T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(44): Show |
54 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.264+9363_264+9378d others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(11): Show |
T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(41): Show |
44 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.264+9361_264+9378d others(20): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(13): Show |
T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.264+9359_264+9378d others(22): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(15): Show |
T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0177 others(6): Show |
9 | HG00558.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+9357_264+9378d others(24): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(17): Show |
T | 10 | a0001c0001t0001g0073 a0001c0001t0001g0227 a0001c0001t0001g0236 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+9355_264+9378d others(26): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(19): Show |
T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01975.hp1 HG02572.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+9353_264+9378d others(28): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(21): Show |
T | 3 | a0001c0001t0001g0254 a0001c0001t0005g0290 a0001c0001t0005g0291 |
3 | HG02965.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.264+9351_264+9378d others(30): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(23): Show |
T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0178 a0001c0001t0001g0197 others(3): Show |
6 | HG02886.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+9349_264+9378d others(32): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316719 | TCACACAC others(25): Show |
T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+9347_264+9378d others(34): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48316719 | ||||||
chr13:48316727 | A | T | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.264+9321A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316727 | |||||||
chr13:48316731 | ACACACAC others(8): Show |
A | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.264+9326_264+9340d others(17): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316731 | |||||||
chr13:48316747 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.264+9341A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316747 | |||||||
chr13:48316854 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.264+9448G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316854 | |||||||
chr13:48316903 | T | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(27): Show |
31 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.264+9497T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316903 | |||||||
chr13:48316951 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+9545T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316951 | |||||||
chr13:48316992 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264+9586T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48316992 | |||||||
chr13:48317100 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
74 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.264+9694A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317100 | |||||||
chr13:48317159 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264+9753G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317159 | |||||||
chr13:48317187 | A | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01069.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264+9781A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317187 | |||||||
chr13:48317278 | A | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(78): Show |
83 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.264+9872A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317278 | |||||||
chr13:48317379 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.264+9973C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317379 | |||||||
chr13:48317383 | G | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0152 a0001c0001t0001g0165 others(6): Show |
9 | HG01074.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.264+9977G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317383 | |||||||
chr13:48317463 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+10057G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317463 | |||||||
chr13:48317506 | C | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.264+10100C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317506 | |||||||
chr13:48317523 | G | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+10117G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317523 | |||||||
chr13:48317700 | G | A | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.264+10294G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317700 | |||||||
chr13:48317791 | G | A | 3 | a0001c0001t0001g0275 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG01069.hp1 HG01071.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.264+10385G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317791 | |||||||
chr13:48317922 | T | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | NA18980.hp1 NA19063.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+10516T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317922 | |||||||
chr13:48317945 | G | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+10539G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317945 | |||||||
chr13:48317956 | C | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.264+10550C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48317956 | |||||||
chr13:48318035 | G | A | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.264+10629G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318035 | |||||||
chr13:48318082 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.264+10676C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318082 | |||||||
chr13:48318141 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.264+10735C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318141 | |||||||
chr13:48318145 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.264+10739C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318145 | |||||||
chr13:48318182 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.264+10776G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318182 | |||||||
chr13:48318393 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.264+10987T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318393 | |||||||
chr13:48318437 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.264+11031C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318437 | |||||||
chr13:48318585 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0047 |
2 | HG00558.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.264+11179C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318585 | |||||||
chr13:48318732 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.264+11326G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318732 | |||||||
chr13:48318757 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.264+11351G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318757 | |||||||
chr13:48318775 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.264+11369T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318775 | |||||||
chr13:48318835 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.264+11429G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318835 | |||||||
chr13:48318856 | T | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.264+11450T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318856 | |||||||
chr13:48318888 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+11482T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318888 | |||||||
chr13:48318929 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.264+11523C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318929 | |||||||
chr13:48318970 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+11564A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48318970 | |||||||
chr13:48319106 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(64): Show |
69 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.264+11700G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319106 | |||||||
chr13:48319111 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.264+11705C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319111 | |||||||
chr13:48319176 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.264+11770G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319176 | |||||||
chr13:48319205 | T | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.264+11799T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319205 | |||||||
chr13:48319376 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+11970G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319376 | |||||||
chr13:48319390 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+11984C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319390 | |||||||
chr13:48319577 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.264+12171G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319577 | |||||||
chr13:48319597 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.264+12191T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319597 | |||||||
chr13:48319647 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+12241T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319647 | |||||||
chr13:48319688 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.264+12282G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319688 | |||||||
chr13:48319700 | GA | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+12295delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319700 | |||||||
chr13:48319876 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+12470C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48319876 | |||||||
chr13:48320008 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.264+12602C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320008 | |||||||
chr13:48320135 | G | A | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+12729G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320135 | |||||||
chr13:48320153 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+12747C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320153 | |||||||
chr13:48320258 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+12852G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320258 | |||||||
chr13:48320292 | C | A | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.264+12886C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320292 | |||||||
chr13:48320388 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.264+12982C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320388 | |||||||
chr13:48320737 | C | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+13331C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320737 | |||||||
chr13:48320771 | C | T | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+13365C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320771 | |||||||
chr13:48320788 | C | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+13382C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320788 | |||||||
chr13:48320837 | G | GA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(28): Show |
33 | HG00323.hp2 HG01109.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.264+13445dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48320837 | ||||||
chr13:48320837 | GA | G | 9 | a0001c0001t0001g0027 a0001c0001t0001g0229 a0001c0001t0001g0254 others(6): Show |
9 | HG01069.hp2 HG01168.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.264+13445delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48320837 | ||||||
chr13:48320936 | G | A | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+13530G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48320936 | |||||||
chr13:48321035 | A | G | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG02486.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+13629A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321035 | |||||||
chr13:48321065 | C | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+13659C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321065 | |||||||
chr13:48321136 | C | A | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.264+13730C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321136 | |||||||
chr13:48321141 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.264+13735C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321141 | |||||||
chr13:48321156 | C | T | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG01192.hp2 HG01975.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.264+13750C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321156 | |||||||
chr13:48321164 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+13758G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321164 | |||||||
chr13:48321170 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.264+13764G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321170 | |||||||
chr13:48321379 | C | T | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.264+13973C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321379 | |||||||
chr13:48321384 | G | A | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG02109.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.264+13978G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321384 | |||||||
chr13:48321431 | A | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+14025A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321431 | |||||||
chr13:48321483 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.264+14077T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321483 | |||||||
chr13:48321534 | C | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.264+14128C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321534 | |||||||
chr13:48321576 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.264+14170C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321576 | |||||||
chr13:48321668 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.264+14262T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321668 | |||||||
chr13:48321868 | C | CA | 21 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(18): Show |
22 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.264+14470dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48321868 | ||||||
chr13:48321968 | T | C | 8 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.264+14562T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48321968 | |||||||
chr13:48322007 | G | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+14601G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322007 | |||||||
chr13:48322040 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.264+14634G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322040 | |||||||
chr13:48322559 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+15153T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322559 | |||||||
chr13:48322573 | G | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+15167G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322573 | |||||||
chr13:48322717 | G | A | 13 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(10): Show |
13 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+15311G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322717 | |||||||
chr13:48322782 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.264+15376T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322782 | |||||||
chr13:48322834 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+15428T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322834 | |||||||
chr13:48322919 | A | AT | 27 | a0001c0001t0001g0061 a0001c0001t0001g0118 a0001c0001t0001g0119 others(24): Show |
27 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.264+15524dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48322919 | ||||||
chr13:48322941 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+15535A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322941 | |||||||
chr13:48322968 | C | T | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+15562C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322968 | |||||||
chr13:48322973 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.264+15567G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48322973 | |||||||
chr13:48323091 | T | G | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | NA18998.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.264+15685T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323091 | |||||||
chr13:48323112 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.264+15706A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323112 | |||||||
chr13:48323170 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.264+15764T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323170 | |||||||
chr13:48323384 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
108 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.264+15978C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323384 | |||||||
chr13:48323481 | TTGATTTT others(26): Show |
T | 1 | a0005c0005t0001g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.264+16077_264+1610 others(37): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48323481 | ||||||
chr13:48323489 | T | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | NA18945.hp1 NA18952.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+16083T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323489 | |||||||
chr13:48323705 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.264+16299T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323705 | |||||||
chr13:48323964 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.264+16558T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48323964 | |||||||
chr13:48324018 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.264+16612G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324018 | |||||||
chr13:48324078 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.264+16672A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324078 | |||||||
chr13:48324127 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0219 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.264+16721A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324127 | |||||||
chr13:48324136 | G | A | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+16730G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324136 | |||||||
chr13:48324139 | A | G | 5 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+16733A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324139 | |||||||
chr13:48324143 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+16737C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324143 | |||||||
chr13:48324179 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.264+16773C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324179 | |||||||
chr13:48324240 | T | C | 18 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+16834T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324240 | |||||||
chr13:48324335 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.264+16929T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324335 | |||||||
chr13:48324424 | G | A | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.264+17018G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324424 | |||||||
chr13:48324428 | AAT | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0060 others(28): Show |
32 | HG00323.hp2 HG00558.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.264+17025_264+1702 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48324428 | ||||||
chr13:48324430 | TA | T | 157 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.264+17025delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324430 | |||||||
chr13:48324431 | A | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
89 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.264+17025A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324431 | |||||||
chr13:48324431 | AT | A | 21 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(18): Show |
21 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.264+17040delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48324431 | ||||||
chr13:48324457 | T | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(79): Show |
84 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.264+17051T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324457 | |||||||
chr13:48324548 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.264+17142G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324548 | |||||||
chr13:48324565 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.264+17159C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324565 | |||||||
chr13:48324658 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.264+17252G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324658 | |||||||
chr13:48324679 | C | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG00099.hp1 HG04228.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.264+17273C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324679 | |||||||
chr13:48324680 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.264+17274A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324680 | |||||||
chr13:48324720 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.264+17314T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324720 | |||||||
chr13:48324843 | G | GT | 33 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(30): Show |
34 | HG00323.hp2 HG00558.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.264+17447dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48324843 | ||||||
chr13:48324850 | T | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
103 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.264+17444T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48324850 | |||||||
chr13:48324850 | TTTTG | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0044 others(70): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.264+17456_264+1745 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48324850 | ||||||
chr13:48324851 | TTTG | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0147 a0001c0001t0001g0151 others(2): Show |
8 | NA18971.hp2 NA18974.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.264+17448_264+1745 others(7): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48324851 | ||||||
chr13:48325001 | CA | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0078 |
3 | NA18956.hp1 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.264+17596delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48325001 | |||||||
chr13:48325078 | AG | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-17519delG | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48325078 | ||||||
chr13:48325193 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-17406A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48325193 | |||||||
chr13:48325242 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.265-17357G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48325242 | |||||||
chr13:48325690 | A | AT | 8 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG03041.hp2 HG03225.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.265-16899dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48325690 | ||||||
chr13:48325690 | AT | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
108 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.265-16899delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48325690 | ||||||
chr13:48326081 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.265-16518T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326081 | |||||||
chr13:48326317 | T | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.265-16282T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326317 | |||||||
chr13:48326525 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-16074C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326525 | |||||||
chr13:48326592 | T | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-16007T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326592 | |||||||
chr13:48326747 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-15852C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326747 | |||||||
chr13:48326875 | C | T | 1 | a0001c0001t0005g0291 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.265-15724C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326875 | |||||||
chr13:48326929 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.265-15670A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326929 | |||||||
chr13:48326938 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-15661T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48326938 | |||||||
chr13:48327099 | GA | G | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
19 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-15499delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327099 | |||||||
chr13:48327182 | A | AT | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
82 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.265-15405dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48327182 | ||||||
chr13:48327239 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.265-15360C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327239 | |||||||
chr13:48327387 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.265-15212T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327387 | |||||||
chr13:48327731 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-14868G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327731 | |||||||
chr13:48327739 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(73): Show |
78 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.265-14860T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327739 | |||||||
chr13:48327825 | A | AT | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-14771dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48327825 | ||||||
chr13:48327829 | C | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-14770C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327829 | |||||||
chr13:48327849 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-14750G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327849 | |||||||
chr13:48327969 | TGAAAAA | T | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-14623_265-1461 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48327969 | ||||||
chr13:48327985 | A | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(59): Show |
64 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.265-14614A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327985 | |||||||
chr13:48327986 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-14613G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48327986 | |||||||
chr13:48328003 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.265-14596C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328003 | |||||||
chr13:48328207 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-14392T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328207 | |||||||
chr13:48328461 | G | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-14138G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328461 | |||||||
chr13:48328470 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265-14129C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328470 | |||||||
chr13:48328481 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-14118G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328481 | |||||||
chr13:48328484 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.265-14115C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48328484 | |||||||
chr13:48328649 | CA | C | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(19): Show |
22 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-13948delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48328649 | ||||||
chr13:48328957 | AT | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.265-13635delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48328957 | ||||||
chr13:48329013 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.265-13586T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329013 | |||||||
chr13:48329080 | A | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.265-13519A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329080 | |||||||
chr13:48329118 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265-13481T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329118 | |||||||
chr13:48329214 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-13385A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329214 | |||||||
chr13:48329391 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.265-13208T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329391 | |||||||
chr13:48329419 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.265-13180G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329419 | |||||||
chr13:48329459 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0182 a0001c0001t0002g0184 others(2): Show |
5 | HG01243.hp1 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-13140G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329459 | |||||||
chr13:48329552 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-13047C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329552 | |||||||
chr13:48329553 | G | A | 76 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(73): Show |
78 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(75): Show |
intron_variant | MODIFIER | c.265-13046G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329553 | |||||||
chr13:48329615 | A | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | NA18945.hp1 NA18952.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-12984A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329615 | |||||||
chr13:48329715 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.265-12884A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329715 | |||||||
chr13:48329724 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.265-12875G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329724 | |||||||
chr13:48329790 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.265-12809G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329790 | |||||||
chr13:48329884 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-12715T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329884 | |||||||
chr13:48329891 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-12708A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329891 | |||||||
chr13:48329895 | A | G | 3 | a0001c0001t0001g0218 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG02622.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.265-12704A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48329895 | |||||||
chr13:48330000 | T | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0228 others(1): Show |
4 | HG00738.hp2 HG01168.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-12599T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330000 | |||||||
chr13:48330077 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-12522C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330077 | |||||||
chr13:48330108 | TA | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0036 others(16): Show |
22 | HG01243.hp2 HG01975.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-12479delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48330108 | ||||||
chr13:48330120 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.265-12479A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330120 | |||||||
chr13:48330149 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.265-12450C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330149 | |||||||
chr13:48330351 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-12248A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330351 | |||||||
chr13:48330373 | C | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.265-12226C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48330373 | |||||||
chr13:48331000 | A | T | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.265-11599A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331000 | |||||||
chr13:48331081 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.265-11518A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331081 | |||||||
chr13:48331087 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-11512T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331087 | |||||||
chr13:48331158 | A | G | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-11441A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331158 | |||||||
chr13:48331372 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.265-11227A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331372 | |||||||
chr13:48331435 | T | A | 1 | a0001c0001t0001g0067 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.265-11164T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331435 | |||||||
chr13:48331500 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.265-11099A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331500 | |||||||
chr13:48331918 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.265-10681A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48331918 | |||||||
chr13:48332107 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.265-10492T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332107 | |||||||
chr13:48332244 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.265-10355T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332244 | |||||||
chr13:48332349 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-10250G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332349 | |||||||
chr13:48332414 | A | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0002c0002t0001g0250 |
3 | HG02717.hp1 HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.265-10185A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332414 | |||||||
chr13:48332601 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.265-9998A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332601 | |||||||
chr13:48332703 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.265-9896G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332703 | |||||||
chr13:48332711 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.265-9888C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332711 | |||||||
chr13:48332743 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0183 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.265-9856G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332743 | |||||||
chr13:48332876 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-9723G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48332876 | |||||||
chr13:48333023 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.265-9576C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333023 | |||||||
chr13:48333148 | A | C | 1 | a0001c0001t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.265-9451A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333148 | |||||||
chr13:48333161 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.265-9438A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333161 | |||||||
chr13:48333171 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0002c0002t0001g0250 others(3): Show |
6 | HG00099.hp1 HG02818.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.265-9428G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333171 | |||||||
chr13:48333299 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-9300G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333299 | |||||||
chr13:48333420 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-9179G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333420 | |||||||
chr13:48333726 | GA | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.265-8865delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48333726 | ||||||
chr13:48333735 | G | GA | 5 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-8855dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48333735 | ||||||
chr13:48333850 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-8749A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48333850 | |||||||
chr13:48334015 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-8584T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334015 | |||||||
chr13:48334214 | G | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-8385G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334214 | |||||||
chr13:48334269 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.265-8330C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334269 | |||||||
chr13:48334411 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-8188A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334411 | |||||||
chr13:48334499 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.265-8100T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334499 | |||||||
chr13:48334517 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.265-8082T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334517 | |||||||
chr13:48334531 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-8068T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334531 | |||||||
chr13:48334666 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.265-7933G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334666 | |||||||
chr13:48334675 | T | G | 1 | a0001c0001t0006g0286 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.265-7924T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334675 | |||||||
chr13:48334724 | T | G | 6 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0154 others(3): Show |
6 | HG04184.hp2 NA18747.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-7875T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334724 | |||||||
chr13:48334751 | A | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.265-7848A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334751 | |||||||
chr13:48334805 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-7794G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48334805 | |||||||
chr13:48334917 | T | TC | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-7681dupC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48334917 | ||||||
chr13:48335021 | G | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-7578G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335021 | |||||||
chr13:48335181 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0065 |
2 | NA18970.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.265-7418A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335181 | |||||||
chr13:48335199 | T | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-7400T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335199 | |||||||
chr13:48335345 | A | G | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.265-7254A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335345 | |||||||
chr13:48335374 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-7225G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335374 | |||||||
chr13:48335396 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.265-7203G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335396 | |||||||
chr13:48335397 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.265-7202T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335397 | |||||||
chr13:48335411 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-7188A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335411 | |||||||
chr13:48335433 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.265-7166A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335433 | |||||||
chr13:48335609 | T | TC | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.265-6990_265-6989i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335609 | |||||||
chr13:48335763 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-6836G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48335763 | |||||||
chr13:48336068 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.265-6531G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336068 | |||||||
chr13:48336091 | G | A | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(19): Show |
22 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-6508G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336091 | |||||||
chr13:48336133 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.265-6466A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336133 | |||||||
chr13:48336146 | C | CT | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-6446dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48336146 | ||||||
chr13:48336168 | A | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0152 a0001c0001t0001g0165 others(6): Show |
9 | HG01074.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.265-6431A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336168 | |||||||
chr13:48336315 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-6284T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336315 | |||||||
chr13:48336422 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.265-6177A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336422 | |||||||
chr13:48336471 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-6128G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336471 | |||||||
chr13:48336489 | T | G | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-6110T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336489 | |||||||
chr13:48336610 | A | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.265-5989A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336610 | |||||||
chr13:48336708 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-5891T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336708 | |||||||
chr13:48336745 | T | TCTTG | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.265-5851_265-5850i others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48336745 | ||||||
chr13:48336813 | G | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-5786G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336813 | |||||||
chr13:48336853 | A | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-5746A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336853 | |||||||
chr13:48336855 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 |
3 | HG02559.hp1 HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.265-5744G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336855 | |||||||
chr13:48336940 | C | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.265-5659C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48336940 | |||||||
chr13:48337127 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.265-5472G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337127 | |||||||
chr13:48337128 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.265-5471T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337128 | |||||||
chr13:48337173 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.265-5426G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337173 | |||||||
chr13:48337196 | C | T | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.265-5403C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337196 | |||||||
chr13:48337263 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-5336A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337263 | |||||||
chr13:48337310 | G | A | 10 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(7): Show |
10 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-5289G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337310 | |||||||
chr13:48337353 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.265-5246T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337353 | |||||||
chr13:48337357 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-5242G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337357 | |||||||
chr13:48337411 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-5188T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337411 | |||||||
chr13:48337526 | T | G | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-5073T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337526 | |||||||
chr13:48337581 | G | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.265-5018G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337581 | |||||||
chr13:48337746 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.265-4853C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337746 | |||||||
chr13:48337747 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.265-4852G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337747 | |||||||
chr13:48337787 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.265-4812C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337787 | |||||||
chr13:48337865 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.265-4734G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337865 | |||||||
chr13:48337940 | G | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG01069.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.265-4659G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48337940 | |||||||
chr13:48338070 | G | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.265-4529G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338070 | |||||||
chr13:48338133 | T | C | 19 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0142 others(16): Show |
19 | HG00099.hp2 HG01243.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-4466T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338133 | |||||||
chr13:48338216 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.265-4383A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338216 | |||||||
chr13:48338236 | G | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-4363G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338236 | |||||||
chr13:48338291 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0099 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.265-4308T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338291 | |||||||
chr13:48338334 | G | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-4265G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338334 | |||||||
chr13:48338370 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-4229A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338370 | |||||||
chr13:48338387 | C | G | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.265-4212C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338387 | |||||||
chr13:48338507 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265-4092C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338507 | |||||||
chr13:48338545 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.265-4054T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338545 | |||||||
chr13:48338603 | G | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-3996G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338603 | |||||||
chr13:48338659 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.265-3940G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338659 | |||||||
chr13:48338807 | T | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-3792T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48338807 | |||||||
chr13:48338866 | CGTTTCT | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.265-3728_265-3723d others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48338866 | ||||||
chr13:48339022 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.265-3577G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339022 | |||||||
chr13:48339124 | A | G | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.265-3475A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339124 | |||||||
chr13:48339175 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-3424G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339175 | |||||||
chr13:48339183 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.265-3416A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339183 | |||||||
chr13:48339192 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.265-3407T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339192 | |||||||
chr13:48339197 | A | T | 1 | a0001c0001t0001g0283 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.265-3402A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339197 | |||||||
chr13:48339236 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.265-3363G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339236 | |||||||
chr13:48339240 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-3359C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339240 | |||||||
chr13:48339249 | C | T | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.265-3350C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339249 | |||||||
chr13:48339250 | G | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-3349G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339250 | |||||||
chr13:48339276 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.265-3323A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339276 | |||||||
chr13:48339287 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.265-3312C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339287 | |||||||
chr13:48339339 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.265-3260C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339339 | |||||||
chr13:48339351 | C | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-3248C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339351 | |||||||
chr13:48339374 | G | A | 4 | a0001c0001t0001g0200 a0001c0001t0003g0004 a0001c0001t0003g0120 others(1): Show |
5 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-3225G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339374 | |||||||
chr13:48339394 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0220 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.265-3205C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339394 | |||||||
chr13:48339441 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.265-3158C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339441 | |||||||
chr13:48339474 | G | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(59): Show |
64 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.265-3125G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339474 | |||||||
chr13:48339641 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.265-2958C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339641 | |||||||
chr13:48339874 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.265-2725T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339874 | |||||||
chr13:48339899 | A | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-2700A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339899 | |||||||
chr13:48339918 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.265-2681C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339918 | |||||||
chr13:48339931 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02145.hp1 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2668G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48339931 | |||||||
chr13:48340088 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-2511T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340088 | |||||||
chr13:48340092 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-2507G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340092 | |||||||
chr13:48340234 | G | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.265-2365G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340234 | |||||||
chr13:48340244 | A | T | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-2355A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340244 | |||||||
chr13:48340430 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.265-2169A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340430 | |||||||
chr13:48340506 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | NA18906.hp1 NA19004.hp1 NA19088.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2093C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340506 | |||||||
chr13:48340560 | CATTTTTT others(1): Show |
C | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(19): Show |
22 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-2036_265-2029d others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48340560 | ||||||
chr13:48340572 | T | C | 22 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(19): Show |
22 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.265-2027T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340572 | |||||||
chr13:48340589 | G | GAA | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.265-2002_265-2001d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48340589 | ||||||
chr13:48340656 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.265-1943A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340656 | |||||||
chr13:48340679 | A | T | 1 | a0001c0001t0007g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265-1920A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340679 | |||||||
chr13:48340726 | GACAA | G | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-1868_265-1865d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48340726 | ||||||
chr13:48340898 | G | A | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.265-1701G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48340898 | |||||||
chr13:48341040 | A | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-1559A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341040 | |||||||
chr13:48341187 | C | A | 8 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
8 | HG01069.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.265-1412C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341187 | |||||||
chr13:48341410 | C | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-1189C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341410 | |||||||
chr13:48341570 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.265-1029C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341570 | |||||||
chr13:48341633 | T | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-966T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341633 | |||||||
chr13:48341682 | T | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-917T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341682 | |||||||
chr13:48341840 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.265-759G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48341840 | |||||||
chr13:48342021 | G | A | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-578G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48342021 | |||||||
chr13:48342036 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.265-563C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48342036 | |||||||
chr13:48342082 | G | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0102 others(4): Show |
7 | HG00609.hp1 NA18948.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-517G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48342082 | |||||||
chr13:48342105 | T | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.265-494T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48342105 | |||||||
chr13:48342352 | CTTATTTA others(1): Show |
C | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-244_265-237del others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr13 | 48342352 | ||||||
chr13:48342367 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.265-232A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 2/26 | chr13 | 48342367 | |||||||
chr13:48342726 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+12T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48342726 | |||||||
chr13:48342751 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.380+37A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48342751 | |||||||
chr13:48342759 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(74): Show |
85 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.380+45C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48342759 | |||||||
chr13:48342907 | G | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+193G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48342907 | |||||||
chr13:48343102 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.380+388A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343102 | |||||||
chr13:48343272 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.380+558T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343272 | |||||||
chr13:48343363 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0077 |
2 | NA18987.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.380+649T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343363 | |||||||
chr13:48343408 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.380+694A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343408 | |||||||
chr13:48343525 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.380+811G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343525 | |||||||
chr13:48343537 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(59): Show |
64 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.380+823A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343537 | |||||||
chr13:48343687 | C | T | 7 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG04184.hp2 NA18747.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.380+973C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48343687 | |||||||
chr13:48344038 | C | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.381-1042C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344038 | |||||||
chr13:48344172 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.381-908C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344172 | |||||||
chr13:48344327 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.381-753C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344327 | |||||||
chr13:48344379 | G | A | 1 | a0001c0001t0007g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.381-701G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344379 | |||||||
chr13:48344379 | G | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.381-701G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344379 | |||||||
chr13:48344495 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.381-585G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344495 | |||||||
chr13:48344666 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.381-414A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344666 | |||||||
chr13:48344828 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.381-252C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344828 | |||||||
chr13:48344893 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.381-187A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344893 | |||||||
chr13:48344928 | A | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(61): Show |
66 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.381-152A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48344928 | |||||||
chr13:48345022 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.381-58G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 3/26 | chr13 | 48345022 | |||||||
chr13:48345222 | T | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.500+23T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345222 | |||||||
chr13:48345370 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.500+171A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345370 | |||||||
chr13:48345398 | A | T | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.500+199A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345398 | |||||||
chr13:48345504 | G | T | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.500+305G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345504 | |||||||
chr13:48345535 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.500+336G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345535 | |||||||
chr13:48345581 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.500+382T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345581 | |||||||
chr13:48345616 | A | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.500+417A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345616 | |||||||
chr13:48345620 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.500+421T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345620 | |||||||
chr13:48345715 | C | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.500+516C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345715 | |||||||
chr13:48345728 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+529G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345728 | |||||||
chr13:48345746 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.500+547G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345746 | |||||||
chr13:48345787 | T | C | 4 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00738.hp1 HG02055.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.500+588T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345787 | |||||||
chr13:48345791 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.500+592G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345791 | |||||||
chr13:48345810 | T | G | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.500+611T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345810 | |||||||
chr13:48345944 | C | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.500+745C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345944 | |||||||
chr13:48345961 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.500+762T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48345961 | |||||||
chr13:48346087 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.500+888A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48346087 | |||||||
chr13:48346099 | C | CT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.500+919dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346099 | ||||||
chr13:48346099 | C | CTT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0138 a0001c0001t0001g0145 others(24): Show |
27 | HG00733.hp1 HG01884.hp2 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.500+918_500+919dup others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346099 | ||||||
chr13:48346099 | C | CTTT | 7 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.500+917_500+919dup others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346099 | ||||||
chr13:48346368 | ATATGTG | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0133 a0001c0001t0001g0136 others(7): Show |
13 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.500+1171_500+1176d others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346368 | ||||||
chr13:48346370 | A | ATG | 5 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0067 others(2): Show |
5 | HG00408.hp2 HG01928.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+1214_500+1215d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATG | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(79): Show |
82 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.500+1214_500+1215d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTG | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0115 others(23): Show |
27 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.500+1212_500+1215d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTG | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(91): Show |
97 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.500+1210_500+1215d others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTGT others(1): Show |
A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0127 others(15): Show |
20 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.500+1208_500+1215d others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTGT others(3): Show |
A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
17 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.500+1206_500+1215d others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTGT others(5): Show |
A | 16 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
17 | HG01192.hp2 HG01243.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.500+1204_500+1215d others(14): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTGT others(7): Show |
A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+1202_500+1215d others(16): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346370 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.500+1200_500+1215d others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346370 | ||||||
chr13:48346372 | G | A | 1 | a0001c0004t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.500+1173G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48346372 | |||||||
chr13:48346433 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.500+1234A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48346433 | |||||||
chr13:48346606 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.501-1219G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48346606 | |||||||
chr13:48346772 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.501-1053C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48346772 | |||||||
chr13:48346956 | GT | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0200 others(27): Show |
31 | HG00323.hp2 HG02129.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.501-858delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr13 | 48346956 | ||||||
chr13:48347075 | T | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.501-750T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347075 | |||||||
chr13:48347188 | G | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.501-637G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347188 | |||||||
chr13:48347289 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501-536C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347289 | |||||||
chr13:48347404 | T | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0126 others(59): Show |
64 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.501-421T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347404 | |||||||
chr13:48347510 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.501-315T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347510 | |||||||
chr13:48347748 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.501-77A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347748 | |||||||
chr13:48347787 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-38G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 4/26 | chr13 | 48347787 | |||||||
chr13:48348161 | G | T | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.539+298G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | chr13 | 48348161 | |||||||
chr13:48348351 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.539+488T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | chr13 | 48348351 | |||||||
chr13:48348594 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(75): Show |
80 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.540-362T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | chr13 | 48348594 | |||||||
chr13:48348646 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0072 |
2 | HG02056.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.540-310A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | chr13 | 48348646 | |||||||
chr13:48348680 | A | AT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0109 others(27): Show |
31 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.540-265dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr13 | 48348680 | ||||||
chr13:48348794 | T | C | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.540-162T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 5/26 | chr13 | 48348794 | |||||||
chr13:48349169 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.607+146A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349169 | |||||||
chr13:48349367 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+344C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349367 | |||||||
chr13:48349415 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.607+392T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349415 | |||||||
chr13:48349470 | T | A | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+447T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349470 | |||||||
chr13:48349626 | GGAAGA | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.607+609_607+613del others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48349626 | ||||||
chr13:48349672 | A | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.607+649A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349672 | |||||||
chr13:48349911 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.607+888A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349911 | |||||||
chr13:48349994 | G | A | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.607+971G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48349994 | |||||||
chr13:48350053 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.607+1030A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350053 | |||||||
chr13:48350078 | A | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.607+1055A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350078 | |||||||
chr13:48350099 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.607+1076G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350099 | |||||||
chr13:48350626 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.607+1603A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350626 | |||||||
chr13:48350713 | G | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.607+1690G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350713 | |||||||
chr13:48350796 | A | AT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.607+1776dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48350796 | ||||||
chr13:48350796 | A | G | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.607+1773A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350796 | |||||||
chr13:48350895 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.607+1872G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48350895 | |||||||
chr13:48351513 | AT | A | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.607+2495delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48351513 | ||||||
chr13:48351679 | A | AT | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+2668dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48351679 | ||||||
chr13:48351834 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.607+2811C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48351834 | |||||||
chr13:48351973 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.607+2950C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48351973 | |||||||
chr13:48351981 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.607+2958C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48351981 | |||||||
chr13:48352158 | T | C | 1 | a0001c0001t0002g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.607+3135T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352158 | |||||||
chr13:48352183 | C | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+3160C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352183 | |||||||
chr13:48352304 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.607+3281C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352304 | |||||||
chr13:48352349 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.607+3326C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352349 | |||||||
chr13:48352368 | GT | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0100 a0001c0001t0001g0118 others(46): Show |
51 | HG00099.hp1 HG00323.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.607+3358delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48352368 | ||||||
chr13:48352374 | T | C | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.607+3351T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352374 | |||||||
chr13:48352381 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.607+3358T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352381 | |||||||
chr13:48352442 | T | G | 29 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(26): Show |
29 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+3419T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352442 | |||||||
chr13:48352678 | C | T | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.607+3655C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352678 | |||||||
chr13:48352782 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.607+3759G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352782 | |||||||
chr13:48352914 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.607+3891G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352914 | |||||||
chr13:48352972 | A | G | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.607+3949A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48352972 | |||||||
chr13:48353201 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.607+4178G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353201 | |||||||
chr13:48353225 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.607+4202G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353225 | |||||||
chr13:48353330 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.607+4307A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353330 | |||||||
chr13:48353451 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.607+4428A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353451 | |||||||
chr13:48353744 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.607+4721T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353744 | |||||||
chr13:48353750 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.607+4727G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353750 | |||||||
chr13:48353774 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0168 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.607+4751C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353774 | |||||||
chr13:48353860 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.607+4837G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353860 | |||||||
chr13:48353915 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.607+4892C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48353915 | |||||||
chr13:48354192 | A | G | 4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0284 others(1): Show |
4 | HG00323.hp2 NA18939.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.607+5169A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48354192 | |||||||
chr13:48354318 | A | G | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.607+5295A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48354318 | |||||||
chr13:48354319 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.607+5296A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48354319 | |||||||
chr13:48354328 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.607+5305G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48354328 | |||||||
chr13:48354886 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.608-5131C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48354886 | |||||||
chr13:48355037 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.608-4980C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355037 | |||||||
chr13:48355204 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.608-4813C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355204 | |||||||
chr13:48355218 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.608-4799G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355218 | |||||||
chr13:48355238 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.608-4779G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355238 | |||||||
chr13:48355643 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.608-4374C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355643 | |||||||
chr13:48355748 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.608-4269A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355748 | |||||||
chr13:48355820 | A | T | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.608-4197A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355820 | |||||||
chr13:48355998 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.608-4019G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48355998 | |||||||
chr13:48356104 | A | G | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-3913A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356104 | |||||||
chr13:48356201 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.608-3816A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356201 | |||||||
chr13:48356208 | A | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-3809A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356208 | |||||||
chr13:48356290 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.608-3727C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356290 | |||||||
chr13:48356325 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.608-3692C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356325 | |||||||
chr13:48356435 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.608-3582A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356435 | |||||||
chr13:48356448 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.608-3569T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356448 | |||||||
chr13:48356558 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-3459T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356558 | |||||||
chr13:48356640 | C | T | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.608-3377C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356640 | |||||||
chr13:48356809 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.608-3208A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356809 | |||||||
chr13:48356835 | C | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
23 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.608-3182C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356835 | |||||||
chr13:48356956 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-3061A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48356956 | |||||||
chr13:48357107 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.608-2910G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357107 | |||||||
chr13:48357113 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.608-2904C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357113 | |||||||
chr13:48357169 | A | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-2848A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357169 | |||||||
chr13:48357342 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-2675G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357342 | |||||||
chr13:48357400 | G | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.608-2617G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357400 | |||||||
chr13:48357476 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0076 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.608-2541C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357476 | |||||||
chr13:48357500 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.608-2517G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357500 | |||||||
chr13:48357543 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.608-2474C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357543 | |||||||
chr13:48357795 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-2222A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357795 | |||||||
chr13:48357843 | T | C | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0142 others(11): Show |
14 | HG00099.hp2 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.608-2174T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357843 | |||||||
chr13:48357875 | G | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(14): Show |
17 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.608-2142G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48357875 | |||||||
chr13:48358086 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-1931G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358086 | |||||||
chr13:48358252 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.608-1765T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358252 | |||||||
chr13:48358385 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.608-1632T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358385 | |||||||
chr13:48358449 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.608-1568T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358449 | |||||||
chr13:48358472 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.608-1545C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358472 | |||||||
chr13:48358605 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.608-1412T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358605 | |||||||
chr13:48358620 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-1397C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358620 | |||||||
chr13:48358669 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.608-1348C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358669 | |||||||
chr13:48358802 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-1215G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358802 | |||||||
chr13:48358826 | A | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-1191A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48358826 | |||||||
chr13:48359020 | A | T | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.608-997A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48359020 | |||||||
chr13:48359393 | A | G | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.608-624A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48359393 | |||||||
chr13:48359436 | TAAATA | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-574_608-570del others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr13 | 48359436 | ||||||
chr13:48359539 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0185 |
2 | NA19005.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.608-478C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 6/26 | chr13 | 48359539 | |||||||
chr13:48360162 | A | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.718+35A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360162 | |||||||
chr13:48360265 | G | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+138G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360265 | |||||||
chr13:48360439 | A | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.718+312A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360439 | |||||||
chr13:48360531 | T | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0057 others(4): Show |
7 | NA18943.hp2 NA18952.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+404T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360531 | |||||||
chr13:48360798 | A | G | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.718+671A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360798 | |||||||
chr13:48360842 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.718+715T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360842 | |||||||
chr13:48360847 | G | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.718+720G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48360847 | |||||||
chr13:48361058 | AG | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(14): Show |
17 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.718+932delG | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48361058 | |||||||
chr13:48361287 | C | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.718+1160C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48361287 | |||||||
chr13:48361659 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.719-1156A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48361659 | |||||||
chr13:48361942 | A | AT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.719-855dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 48361942 | ||||||
chr13:48361942 | A | ATT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0142 others(25): Show |
29 | HG00323.hp2 HG02056.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.719-856_719-855dup others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 48361942 | ||||||
chr13:48361974 | A | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02145.hp1 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.719-841A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48361974 | |||||||
chr13:48361986 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.719-829G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48361986 | |||||||
chr13:48362010 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(2): Show |
7 | HG02074.hp2 NA18943.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-805C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48362010 | |||||||
chr13:48362148 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.719-667G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48362148 | |||||||
chr13:48362303 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.719-512A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48362303 | |||||||
chr13:48362315 | AT | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.719-490delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 48362315 | ||||||
chr13:48362332 | C | T | 15 | a0001c0001t0001g0115 a0001c0001t0001g0125 a0001c0001t0001g0126 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.719-483C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48362332 | |||||||
chr13:48362492 | CT | C | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.719-315delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr13 | 48362492 | ||||||
chr13:48362637 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-178T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 7/26 | chr13 | 48362637 | |||||||
chr13:48363090 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.861+133A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363090 | |||||||
chr13:48363124 | A | G | 9 | a0001c0001t0001g0132 a0001c0001t0001g0152 a0001c0001t0001g0165 others(6): Show |
9 | HG01074.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.861+167A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363124 | |||||||
chr13:48363203 | A | AG | 6 | a0001c0001t0001g0119 a0001c0001t0001g0254 a0001c0001t0001g0255 others(3): Show |
6 | HG00099.hp1 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+247dupG | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr13 | 48363203 | ||||||
chr13:48363204 | G | GT | 8 | a0001c0001t0001g0197 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02647.hp1 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.861+262dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr13 | 48363204 | ||||||
chr13:48363204 | GT | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
81 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.861+262delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr13 | 48363204 | ||||||
chr13:48363205 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.861+248T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363205 | |||||||
chr13:48363447 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.861+490C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363447 | |||||||
chr13:48363462 | C | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.861+505C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363462 | |||||||
chr13:48363483 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.861+526G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363483 | |||||||
chr13:48363601 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.861+644T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363601 | |||||||
chr13:48363665 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.861+708A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363665 | |||||||
chr13:48363760 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.861+803A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363760 | |||||||
chr13:48363767 | A | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.861+810A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363767 | |||||||
chr13:48363833 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.861+876A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48363833 | |||||||
chr13:48364148 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.862-746C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364148 | |||||||
chr13:48364149 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.862-745G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364149 | |||||||
chr13:48364268 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.862-626G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364268 | |||||||
chr13:48364363 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0105 |
2 | NA18950.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.862-531G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364363 | |||||||
chr13:48364519 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.862-375T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364519 | |||||||
chr13:48364654 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.862-240G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364654 | |||||||
chr13:48364711 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.862-183T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364711 | |||||||
chr13:48364722 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0041 others(1): Show |
4 | HG02129.hp2 HG02165.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.862-172A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364722 | |||||||
chr13:48364735 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.862-159C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364735 | |||||||
chr13:48364761 | TA | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0035 others(1): Show |
4 | HG01069.hp2 HG03491.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-127delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr13 | 48364761 | ||||||
chr13:48364844 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.862-50A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364844 | |||||||
chr13:48364879 | C | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.862-15C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 8/26 | chr13 | 48364879 | |||||||
chr13:48365058 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+87T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365058 | |||||||
chr13:48365095 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.939+124G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365095 | |||||||
chr13:48365278 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+307C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365278 | |||||||
chr13:48365284 | A | G | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.939+313A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365284 | |||||||
chr13:48365536 | A | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+565A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365536 | |||||||
chr13:48365616 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.939+645T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365616 | |||||||
chr13:48365779 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.939+808A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365779 | |||||||
chr13:48365981 | A | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+1010A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48365981 | |||||||
chr13:48366150 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.939+1179C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48366150 | |||||||
chr13:48366171 | CTTGTTAC others(5): Show |
C | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.939+1204_939+1215d others(14): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr13 | 48366171 | ||||||
chr13:48366197 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.939+1226C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48366197 | |||||||
chr13:48366288 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.940-1206T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48366288 | |||||||
chr13:48366710 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.940-784A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48366710 | |||||||
chr13:48367044 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-450C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367044 | |||||||
chr13:48367102 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(30): Show |
34 | HG00323.hp2 HG00558.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.940-392G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367102 | |||||||
chr13:48367117 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.940-377T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367117 | |||||||
chr13:48367118 | C | CA | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.940-356dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr13 | 48367118 | ||||||
chr13:48367118 | C | CAA | 33 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(30): Show |
34 | HG00673.hp1 HG00673.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.940-357_940-356dup others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr13 | 48367118 | ||||||
chr13:48367119 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.940-375A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367119 | |||||||
chr13:48367282 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.940-212C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367282 | |||||||
chr13:48367330 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.940-164C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367330 | |||||||
chr13:48367331 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.940-163C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367331 | |||||||
chr13:48367383 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.940-111C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 9/26 | chr13 | 48367383 | |||||||
chr13:48367661 | G | A | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1049+58G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48367661 | |||||||
chr13:48367661 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1049+58G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48367661 | |||||||
chr13:48367869 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1049+266A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48367869 | |||||||
chr13:48367873 | G | A | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1049+270G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48367873 | |||||||
chr13:48367954 | A | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0289 |
3 | HG01975.hp1 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1049+351A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48367954 | |||||||
chr13:48368007 | A | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1049+404A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48368007 | |||||||
chr13:48368048 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1049+445C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48368048 | |||||||
chr13:48368076 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0280 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1050-451G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 10/26 | chr13 | 48368076 | |||||||
chr13:48368678 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1127+74C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48368678 | |||||||
chr13:48368810 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1127+206G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48368810 | |||||||
chr13:48368810 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1127+206G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48368810 | |||||||
chr13:48368994 | G | A | 1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1127+390G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48368994 | |||||||
chr13:48369001 | C | T | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1127+397C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369001 | |||||||
chr13:48369006 | CA | C | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127+412delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 48369006 | ||||||
chr13:48369012 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1127+408A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369012 | |||||||
chr13:48369024 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0186 a0001c0001t0001g0188 |
3 | HG00099.hp2 HG03669.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1127+420A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369024 | |||||||
chr13:48369473 | T | C | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1127+869T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369473 | |||||||
chr13:48369821 | C | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0078 |
3 | NA18956.hp1 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1127+1217C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369821 | |||||||
chr13:48369863 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1127+1259T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369863 | |||||||
chr13:48369913 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1127+1309A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48369913 | |||||||
chr13:48370149 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1127+1545C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370149 | |||||||
chr13:48370236 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1127+1632C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370236 | |||||||
chr13:48370272 | A | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1127+1668A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370272 | |||||||
chr13:48370356 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1127+1752C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370356 | |||||||
chr13:48370594 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1127+1990G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370594 | |||||||
chr13:48370802 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1127+2198C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48370802 | |||||||
chr13:48371012 | A | G | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1128-2393A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371012 | |||||||
chr13:48371039 | G | A | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1128-2366G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371039 | |||||||
chr13:48371118 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-2287T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371118 | |||||||
chr13:48371128 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18951.hp2 NA19066.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1128-2277G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371128 | |||||||
chr13:48371537 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1128-1868A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371537 | |||||||
chr13:48371633 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1128-1772C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371633 | |||||||
chr13:48371799 | A | G | 2 | a0001c0001t0001g0289 a0001c0001t0008g0274 |
2 | HG01975.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1128-1606A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371799 | |||||||
chr13:48371834 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0005g0290 a0001c0001t0005g0291 others(2): Show |
5 | HG02886.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128-1571G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371834 | |||||||
chr13:48371912 | C | T | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128-1493C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371912 | |||||||
chr13:48371961 | C | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128-1444C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48371961 | |||||||
chr13:48372080 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1128-1325A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372080 | |||||||
chr13:48372082 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1128-1323G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372082 | |||||||
chr13:48372144 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-1261T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372144 | |||||||
chr13:48372262 | A | G | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-1143A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372262 | |||||||
chr13:48372298 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1128-1107G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372298 | |||||||
chr13:48372377 | G | C | 1 | a0001c0001t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1128-1028G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372377 | |||||||
chr13:48372455 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1128-950C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372455 | |||||||
chr13:48372576 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1128-829G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372576 | |||||||
chr13:48372607 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128-798C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372607 | |||||||
chr13:48372626 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1128-779G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372626 | |||||||
chr13:48372629 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(44): Show |
48 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1128-776C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372629 | |||||||
chr13:48372650 | C | CA | 19 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0118 others(16): Show |
20 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1128-743dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr13 | 48372650 | ||||||
chr13:48372684 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1128-721G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372684 | |||||||
chr13:48372854 | G | T | 14 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1128-551G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372854 | |||||||
chr13:48372857 | C | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1128-548C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372857 | |||||||
chr13:48372951 | A | G | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1128-454A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48372951 | |||||||
chr13:48373333 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1128-72G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48373333 | |||||||
chr13:48373333 | G | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1128-72G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 11/26 | chr13 | 48373333 | |||||||
chr13:48373693 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1215+201T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48373693 | |||||||
chr13:48373712 | G | A | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+220G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48373712 | |||||||
chr13:48373854 | A | G | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1215+362A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48373854 | |||||||
chr13:48373902 | C | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1215+410C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48373902 | |||||||
chr13:48374197 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1215+705G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374197 | |||||||
chr13:48374281 | A | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1215+789A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374281 | |||||||
chr13:48374433 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1215+941A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374433 | |||||||
chr13:48374495 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1215+1003A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374495 | |||||||
chr13:48374798 | T | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+1306T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374798 | |||||||
chr13:48374903 | C | A | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1215+1411C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374903 | |||||||
chr13:48374926 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1215+1434T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48374926 | |||||||
chr13:48375010 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1215+1518C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375010 | |||||||
chr13:48375269 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1216-1649T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375269 | |||||||
chr13:48375530 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1216-1388C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375530 | |||||||
chr13:48375576 | T | TTA | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1328_1216-132 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr13 | 48375576 | ||||||
chr13:48375590 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1216-1328A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375590 | |||||||
chr13:48375771 | GT | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1216-1144delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr13 | 48375771 | ||||||
chr13:48375804 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1216-1114C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375804 | |||||||
chr13:48375809 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1216-1109C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375809 | |||||||
chr13:48375917 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1216-1001T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375917 | |||||||
chr13:48375997 | T | C | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1216-921T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48375997 | |||||||
chr13:48376057 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1216-861G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376057 | |||||||
chr13:48376334 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1216-584C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376334 | |||||||
chr13:48376416 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1216-502C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376416 | |||||||
chr13:48376439 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1216-479G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376439 | |||||||
chr13:48376499 | C | CA | 18 | a0001c0001t0001g0020 a0001c0001t0001g0073 a0001c0001t0001g0080 others(15): Show |
18 | HG00099.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1216-398dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr13 | 48376499 | ||||||
chr13:48376499 | CA | C | 27 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(24): Show |
27 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1216-398delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr13 | 48376499 | ||||||
chr13:48376499 | CAA | C | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-399_1216-398d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr13 | 48376499 | ||||||
chr13:48376571 | C | T | 2 | a0001c0001t0004g0238 a0001c0001t0004g0246 |
2 | HG02630.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1216-347C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376571 | |||||||
chr13:48376688 | G | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0035 others(1): Show |
4 | HG01069.hp2 HG03491.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-230G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376688 | |||||||
chr13:48376889 | A | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1216-29A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 12/26 | chr13 | 48376889 | |||||||
chr13:48377218 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1332+184C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377218 | |||||||
chr13:48377219 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0242 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1332+185C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377219 | |||||||
chr13:48377460 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1332+426T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377460 | |||||||
chr13:48377572 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1332+538G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377572 | |||||||
chr13:48377641 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1332+607G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377641 | |||||||
chr13:48377900 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1332+866G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48377900 | |||||||
chr13:48378253 | C | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(11): Show |
14 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1332+1219C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378253 | |||||||
chr13:48378432 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1333-1162G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378432 | |||||||
chr13:48378498 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0072 |
2 | HG02056.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1333-1096T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378498 | |||||||
chr13:48378580 | C | CT | 5 | a0001c0001t0001g0068 a0001c0001t0001g0289 a0001c0001t0003g0004 others(2): Show |
6 | HG01192.hp2 HG01975.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1333-1000dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 48378580 | ||||||
chr13:48378661 | A | G | 1 | a0001c0001t0001g0014 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1333-933A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378661 | |||||||
chr13:48378706 | A | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-888A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378706 | |||||||
chr13:48378793 | T | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1333-801T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48378793 | |||||||
chr13:48379196 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1333-398A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48379196 | |||||||
chr13:48379201 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1333-393T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48379201 | |||||||
chr13:48379238 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1333-356G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48379238 | |||||||
chr13:48379278 | C | T | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1333-316C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48379278 | |||||||
chr13:48379519 | C | CA | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.1333-61dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr13 | 48379519 | ||||||
chr13:48379565 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1333-29C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 13/26 | chr13 | 48379565 | |||||||
chr13:48379690 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1389+40G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | chr13 | 48379690 | |||||||
chr13:48379818 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1389+168G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | chr13 | 48379818 | |||||||
chr13:48379841 | TC | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+194delC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr13 | 48379841 | ||||||
chr13:48379881 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1390-172A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | chr13 | 48379881 | |||||||
chr13:48379885 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1390-168G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | chr13 | 48379885 | |||||||
chr13:48379957 | T | TA | 40 | a0001c0001t0001g0026 a0001c0001t0001g0072 a0001c0001t0001g0073 others(37): Show |
40 | HG00099.hp1 HG00642.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1390-70dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr13 | 48379957 | ||||||
chr13:48379957 | TA | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0112 others(53): Show |
58 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1390-70delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr13 | 48379957 | ||||||
chr13:48380023 | C | CT | 12 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(9): Show |
12 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1390-17dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr13 | 48380023 | ||||||
chr13:48380042 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1390-11A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 14/26 | chr13 | 48380042 | |||||||
chr13:48380093 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1421+9T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 15/26 | chr13 | 48380093 | |||||||
chr13:48380111 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0168 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1421+27T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 15/26 | chr13 | 48380111 | |||||||
chr13:48380146 | CT | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
6 | NA18943.hp1 NA18948.hp1 NA18960.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1422-8delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr13 | 48380146 | ||||||
chr13:48380306 | T | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+65T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | chr13 | 48380306 | |||||||
chr13:48380314 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1498+73G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | chr13 | 48380314 | |||||||
chr13:48380415 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1498+174T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | chr13 | 48380415 | |||||||
chr13:48381065 | T | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1499-182T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | chr13 | 48381065 | |||||||
chr13:48381130 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1499-117T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | chr13 | 48381130 | |||||||
chr13:48381183 | CA | C | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1499-57delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr13 | 48381183 | ||||||
chr13:48381523 | C | CAA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1695+81_1695+82ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48381523 | ||||||
chr13:48381540 | T | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1695+97T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381540 | |||||||
chr13:48381590 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1695+147A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381590 | |||||||
chr13:48381654 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1695+211A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381654 | |||||||
chr13:48381716 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1695+273T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381716 | |||||||
chr13:48381904 | TCTC | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
260 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1695+462_1695+464d others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381904 | |||||||
chr13:48381977 | A | G | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | NA18971.hp1 NA18975.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1695+534A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48381977 | |||||||
chr13:48382006 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1695+563C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382006 | |||||||
chr13:48382172 | C | T | 8 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00558.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1695+729C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382172 | |||||||
chr13:48382340 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1695+897C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382340 | |||||||
chr13:48382346 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1695+903C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382346 | |||||||
chr13:48382452 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+1009T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382452 | |||||||
chr13:48382518 | A | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1695+1075A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382518 | |||||||
chr13:48382521 | T | C | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1695+1078T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382521 | |||||||
chr13:48382522 | T | C | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1695+1079T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382522 | |||||||
chr13:48382525 | A | G | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1695+1082A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382525 | |||||||
chr13:48382774 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+1331C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382774 | |||||||
chr13:48382853 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1695+1410T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382853 | |||||||
chr13:48382872 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+1429C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382872 | |||||||
chr13:48382876 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+1433G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382876 | |||||||
chr13:48382917 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1695+1474G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48382917 | |||||||
chr13:48383319 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1695+1876A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48383319 | |||||||
chr13:48383432 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+1989G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48383432 | |||||||
chr13:48383932 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1695+2489T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48383932 | |||||||
chr13:48384180 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+2737C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384180 | |||||||
chr13:48384542 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+3099A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384542 | |||||||
chr13:48384647 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1695+3204G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384647 | |||||||
chr13:48384683 | GCTTA | G | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+3244_1695+324 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48384683 | ||||||
chr13:48384723 | C | T | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1695+3280C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384723 | |||||||
chr13:48384727 | A | G | 1 | a0002c0002t0001g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1695+3284A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384727 | |||||||
chr13:48384901 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1695+3458A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48384901 | |||||||
chr13:48385232 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02145.hp1 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+3789C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48385232 | |||||||
chr13:48385614 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+4171G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48385614 | |||||||
chr13:48385747 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+4304G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48385747 | |||||||
chr13:48385964 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+4521G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48385964 | |||||||
chr13:48386041 | T | TA | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1695+4615dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48386041 | ||||||
chr13:48386041 | T | TAA | 60 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0125 others(57): Show |
62 | HG00323.hp2 HG00609.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.1695+4614_1695+461 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48386041 | ||||||
chr13:48386069 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.1695+4626A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386069 | |||||||
chr13:48386126 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1695+4683C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386126 | |||||||
chr13:48386255 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1695+4812G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386255 | |||||||
chr13:48386299 | G | T | 14 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(11): Show |
14 | HG01109.hp2 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1695+4856G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386299 | |||||||
chr13:48386364 | A | AT | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.1695+4931dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48386364 | ||||||
chr13:48386509 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+5066C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386509 | |||||||
chr13:48386718 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+5275G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386718 | |||||||
chr13:48386883 | C | T | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1695+5440C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386883 | |||||||
chr13:48386891 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1695+5448G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386891 | |||||||
chr13:48386930 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1695+5487G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386930 | |||||||
chr13:48386978 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1695+5535A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48386978 | |||||||
chr13:48387007 | A | AGTTTTGG others(1): Show |
3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+5567_1695+557 others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48387007 | ||||||
chr13:48387015 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+5572C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387015 | |||||||
chr13:48387046 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1695+5603C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387046 | |||||||
chr13:48387092 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+5649A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387092 | |||||||
chr13:48387213 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+5770A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387213 | |||||||
chr13:48387229 | A | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1695+5786A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387229 | |||||||
chr13:48387717 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0048 |
2 | HG01361.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1695+6274G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387717 | |||||||
chr13:48387827 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0231 a0001c0001t0001g0232 others(30): Show |
34 | HG00323.hp2 HG00558.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.1695+6384C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387827 | |||||||
chr13:48387918 | A | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+6475A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48387918 | |||||||
chr13:48388027 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1695+6584G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388027 | |||||||
chr13:48388154 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1695+6711C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388154 | |||||||
chr13:48388274 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+6831G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388274 | |||||||
chr13:48388356 | A | G | 9 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1695+6913A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388356 | |||||||
chr13:48388365 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1695+6922T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388365 | |||||||
chr13:48388460 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1695+7017T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388460 | |||||||
chr13:48388549 | T | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+7106T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388549 | |||||||
chr13:48388972 | C | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1695+7529C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48388972 | |||||||
chr13:48389007 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+7564A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389007 | |||||||
chr13:48389084 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0242 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1695+7641C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389084 | |||||||
chr13:48389128 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1695+7685C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389128 | |||||||
chr13:48389175 | A | T | 6 | a0001c0001t0001g0061 a0001c0001t0001g0106 a0001c0001t0001g0108 others(3): Show |
6 | HG00099.hp1 HG01255.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1695+7732A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389175 | |||||||
chr13:48389180 | T | A | 18 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0001t0001g0122 others(15): Show |
19 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1695+7737T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389180 | |||||||
chr13:48389648 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+8205T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389648 | |||||||
chr13:48389648 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+8205T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389648 | |||||||
chr13:48389732 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+8289G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389732 | |||||||
chr13:48389944 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1695+8501C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389944 | |||||||
chr13:48389945 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1695+8502G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48389945 | |||||||
chr13:48390060 | T | C | 9 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1695+8617T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390060 | |||||||
chr13:48390349 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1695+8906A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390349 | |||||||
chr13:48390351 | A | G | 7 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0145 others(4): Show |
7 | HG04184.hp2 NA18747.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+8908A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390351 | |||||||
chr13:48390372 | C | T | 16 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0236 others(13): Show |
16 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1695+8929C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390372 | |||||||
chr13:48390425 | A | G | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1695+8982A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390425 | |||||||
chr13:48390469 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1695+9026A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390469 | |||||||
chr13:48390499 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+9056G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390499 | |||||||
chr13:48390552 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1695+9109A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390552 | |||||||
chr13:48390612 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1695+9169T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390612 | |||||||
chr13:48390689 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1695+9246T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390689 | |||||||
chr13:48390712 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG00609.hp1 NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1695+9269C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390712 | |||||||
chr13:48390727 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1695+9284G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390727 | |||||||
chr13:48390765 | C | T | 15 | a0001c0001t0001g0261 a0001c0001t0001g0265 a0001c0001t0001g0266 others(12): Show |
15 | HG00323.hp2 HG02155.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1695+9322C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390765 | |||||||
chr13:48390846 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1695+9403T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390846 | |||||||
chr13:48390881 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+9438A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48390881 | |||||||
chr13:48391252 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1695+9809A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391252 | |||||||
chr13:48391297 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+9854T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391297 | |||||||
chr13:48391311 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+9868C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391311 | |||||||
chr13:48391367 | A | G | 7 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 others(4): Show |
8 | HG01192.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1695+9924A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391367 | |||||||
chr13:48391444 | G | C | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1695+10001G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391444 | |||||||
chr13:48391449 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1695+10006C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391449 | |||||||
chr13:48391575 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1695+10132C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391575 | |||||||
chr13:48391680 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+10237G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391680 | |||||||
chr13:48391692 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1695+10249C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391692 | |||||||
chr13:48391722 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+10279G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391722 | |||||||
chr13:48391838 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0131 |
2 | HG00741.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1695+10395C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391838 | |||||||
chr13:48391853 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+10410G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391853 | |||||||
chr13:48391903 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1695+10460A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48391903 | |||||||
chr13:48392088 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+10645A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392088 | |||||||
chr13:48392213 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+10770C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392213 | |||||||
chr13:48392750 | TTCTC | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
239 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.1695+11321_1695+11 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48392750 | ||||||
chr13:48392784 | A | G | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1695+11341A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392784 | |||||||
chr13:48392833 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+11390T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392833 | |||||||
chr13:48392871 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0072 |
2 | HG02056.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1695+11428G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392871 | |||||||
chr13:48392941 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+11498T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392941 | |||||||
chr13:48392981 | A | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+11538A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48392981 | |||||||
chr13:48393053 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1695+11610G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48393053 | |||||||
chr13:48393094 | T | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1695+11651T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48393094 | |||||||
chr13:48393473 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+12030C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48393473 | |||||||
chr13:48393779 | AT | A | 9 | a0001c0001t0001g0132 a0001c0001t0001g0152 a0001c0001t0001g0165 others(6): Show |
9 | HG01074.hp2 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1695+12340delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48393779 | ||||||
chr13:48393899 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1695+12456T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48393899 | |||||||
chr13:48394011 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+12568C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394011 | |||||||
chr13:48394095 | C | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG02145.hp1 HG02922.hp1 NA18906.hp1 others(7): Show |
intron_variant | MODIFIER | c.1695+12652C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394095 | |||||||
chr13:48394134 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+12691C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394134 | |||||||
chr13:48394249 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1695+12806G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394249 | |||||||
chr13:48394381 | C | G | 1 | a0001c0001t0003g0120 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1695+12938C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394381 | |||||||
chr13:48394388 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+12945T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394388 | |||||||
chr13:48394417 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+12974C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394417 | |||||||
chr13:48394425 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1695+12982G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394425 | |||||||
chr13:48394460 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1695+13017C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394460 | |||||||
chr13:48394465 | C | T | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1695+13022C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394465 | |||||||
chr13:48394547 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1695+13104G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394547 | |||||||
chr13:48394577 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1695+13134T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394577 | |||||||
chr13:48394604 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1695+13161C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394604 | |||||||
chr13:48394638 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(185): Show |
196 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1695+13195A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394638 | |||||||
chr13:48394670 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+13227C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394670 | |||||||
chr13:48394672 | G | T | 1 | a0001c0001t0005g0292 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1695+13229G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394672 | |||||||
chr13:48394733 | G | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1695+13290G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394733 | |||||||
chr13:48394790 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1695+13347C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394790 | |||||||
chr13:48394857 | A | G | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+13414A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48394857 | |||||||
chr13:48395026 | T | C | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+13583T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395026 | |||||||
chr13:48395070 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1695+13627C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395070 | |||||||
chr13:48395093 | A | AT | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1695+13650_1695+13 others(7): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395093 | |||||||
chr13:48395218 | G | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+13775G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395218 | |||||||
chr13:48395247 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1695+13804T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395247 | |||||||
chr13:48395252 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0065 |
2 | NA18970.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1695+13809A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395252 | |||||||
chr13:48395255 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1695+13812A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395255 | |||||||
chr13:48395269 | G | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+13826G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395269 | |||||||
chr13:48395331 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1695+13888C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395331 | |||||||
chr13:48395379 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1695+13936T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395379 | |||||||
chr13:48395387 | T | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1695+13944T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395387 | |||||||
chr13:48395412 | G | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0076 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1695+13969G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395412 | |||||||
chr13:48395495 | G | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+14052G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395495 | |||||||
chr13:48395522 | G | GAGAAGAA others(5): Show |
1 | a0001c0001t0001g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1695+14081_1695+14 others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48395522 | ||||||
chr13:48395565 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1695+14122C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395565 | |||||||
chr13:48395686 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+14243A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395686 | |||||||
chr13:48395735 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1695+14292A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395735 | |||||||
chr13:48395967 | A | T | 1 | a0001c0001t0001g0296 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1695+14524A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48395967 | |||||||
chr13:48396153 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1695+14710T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396153 | |||||||
chr13:48396186 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1695+14743C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396186 | |||||||
chr13:48396292 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+14849A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396292 | |||||||
chr13:48396363 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1695+14920T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396363 | |||||||
chr13:48396642 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+15199C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396642 | |||||||
chr13:48396827 | G | A | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1695+15384G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396827 | |||||||
chr13:48396888 | GA | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+15452delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48396888 | ||||||
chr13:48396940 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+15497G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396940 | |||||||
chr13:48396968 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1695+15525T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48396968 | |||||||
chr13:48397088 | G | A | 16 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
16 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1695+15645G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397088 | |||||||
chr13:48397095 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
86 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1695+15652C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397095 | |||||||
chr13:48397125 | C | G | 4 | a0001c0001t0001g0137 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | NA18980.hp1 NA19063.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+15682C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397125 | |||||||
chr13:48397168 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1695+15725T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397168 | |||||||
chr13:48397195 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1695+15752A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397195 | |||||||
chr13:48397483 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+16040G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397483 | |||||||
chr13:48397491 | CAG | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | NA18952.hp2 NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1695+16049_1695+16 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397491 | |||||||
chr13:48397501 | G | A | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+16058G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397501 | |||||||
chr13:48397556 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+16113T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397556 | |||||||
chr13:48397650 | C | G | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+16207C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397650 | |||||||
chr13:48397671 | CTTTCAAA others(6): Show |
C | 4 | a0001c0001t0001g0289 a0001c0001t0003g0004 a0001c0001t0003g0120 others(1): Show |
5 | HG01192.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+16238_1695+16 others(19): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48397671 | ||||||
chr13:48397800 | G | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1695+16357G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397800 | |||||||
chr13:48397882 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1695+16439A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48397882 | |||||||
chr13:48398177 | A | G | 1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1695+16734A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398177 | |||||||
chr13:48398233 | T | TA | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1695+16796dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48398233 | ||||||
chr13:48398280 | C | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0078 |
3 | NA18956.hp1 NA19005.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1695+16837C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398280 | |||||||
chr13:48398292 | A | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1695+16849A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398292 | |||||||
chr13:48398417 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1695+16974T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398417 | |||||||
chr13:48398430 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1695+16987A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398430 | |||||||
chr13:48398469 | T | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+17026T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398469 | |||||||
chr13:48398475 | C | T | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
239 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.1695+17032C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398475 | |||||||
chr13:48398744 | C | T | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+17301C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398744 | |||||||
chr13:48398865 | G | T | 2 | a0003c0003t0001g0210 a0003c0003t0001g0211 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1695+17422G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398865 | |||||||
chr13:48398961 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1695+17518G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48398961 | |||||||
chr13:48399133 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1695+17690G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399133 | |||||||
chr13:48399159 | C | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1695+17716C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399159 | |||||||
chr13:48399427 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG04115.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1695+17984T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399427 | |||||||
chr13:48399536 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+18093G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399536 | |||||||
chr13:48399708 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1695+18265T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399708 | |||||||
chr13:48399795 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1695+18352A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399795 | |||||||
chr13:48399866 | A | G | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG03041.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+18423A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399866 | |||||||
chr13:48399905 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+18462T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48399905 | |||||||
chr13:48400353 | A | C | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1695+18910A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48400353 | |||||||
chr13:48400407 | A | T | 24 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(21): Show |
24 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1695+18964A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48400407 | |||||||
chr13:48400606 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
109 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1695+19163G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48400606 | |||||||
chr13:48400718 | T | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0283 |
2 | NA18945.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1695+19275T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48400718 | |||||||
chr13:48400928 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1695+19485C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48400928 | |||||||
chr13:48401102 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1695+19659A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401102 | |||||||
chr13:48401163 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1695+19720T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401163 | |||||||
chr13:48401175 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1695+19732A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401175 | |||||||
chr13:48401204 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0283 |
2 | NA18945.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1695+19761G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401204 | |||||||
chr13:48401410 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1695+19967G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401410 | |||||||
chr13:48401580 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1695+20137A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401580 | |||||||
chr13:48401604 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1695+20161A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401604 | |||||||
chr13:48401652 | G | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.1695+20209G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401652 | |||||||
chr13:48401749 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1695+20306G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401749 | |||||||
chr13:48401770 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1695+20327T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401770 | |||||||
chr13:48401875 | A | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+20432A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48401875 | |||||||
chr13:48402379 | C | CTTTTTTT others(1): Show |
15 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0083 others(12): Show |
15 | HG00323.hp1 HG01074.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1695+20942_1695+20 others(14): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48402379 | ||||||
chr13:48402379 | C | CTTTTTTT others(2): Show |
225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.1695+20941_1695+20 others(15): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48402379 | ||||||
chr13:48402379 | C | CTTTTTTT others(3): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0131 a0001c0001t0001g0151 others(10): Show |
13 | HG00558.hp2 HG00741.hp1 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.1695+20940_1695+20 others(16): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48402379 | ||||||
chr13:48402379 | C | CTTTTTTT others(5): Show |
4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+20938_1695+20 others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48402379 | ||||||
chr13:48402379 | CT | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+20949delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48402379 | ||||||
chr13:48402537 | C | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
104 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1695+21094C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402537 | |||||||
chr13:48402602 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
79 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1695+21159C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402602 | |||||||
chr13:48402691 | A | G | 20 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1695+21248A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402691 | |||||||
chr13:48402719 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
79 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1695+21276A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402719 | |||||||
chr13:48402730 | T | A | 7 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 others(4): Show |
8 | HG01192.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1695+21287T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402730 | |||||||
chr13:48402939 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1695+21496T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48402939 | |||||||
chr13:48403320 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1695+21877C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403320 | |||||||
chr13:48403371 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+21928C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403371 | |||||||
chr13:48403431 | A | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1695+21988A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403431 | |||||||
chr13:48403502 | A | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1695+22059A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403502 | |||||||
chr13:48403522 | C | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1695+22079C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403522 | |||||||
chr13:48403597 | G | A | 16 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
16 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1695+22154G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403597 | |||||||
chr13:48403630 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1695+22187A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48403630 | |||||||
chr13:48404009 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1695+22566A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404009 | |||||||
chr13:48404111 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1695+22668T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404111 | |||||||
chr13:48404153 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1695+22710C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404153 | |||||||
chr13:48404261 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+22818G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404261 | |||||||
chr13:48404442 | GA | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1695+23009delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48404442 | ||||||
chr13:48404530 | CTT | C | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0282 |
3 | HG02129.hp1 NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1695+23091_1695+23 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48404530 | ||||||
chr13:48404579 | T | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1695+23136T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404579 | |||||||
chr13:48404601 | A | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1695+23158A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404601 | |||||||
chr13:48404767 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+23324C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404767 | |||||||
chr13:48404794 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1695+23351G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48404794 | |||||||
chr13:48405031 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
79 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1695+23588T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405031 | |||||||
chr13:48405099 | T | C | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1695+23656T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405099 | |||||||
chr13:48405108 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+23665A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405108 | |||||||
chr13:48405172 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1695+23729A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405172 | |||||||
chr13:48405188 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+23745A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405188 | |||||||
chr13:48405220 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1695+23777C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405220 | |||||||
chr13:48405237 | G | C | 1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1695+23794G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405237 | |||||||
chr13:48405369 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1695+23926C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405369 | |||||||
chr13:48405487 | A | C | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+24044A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405487 | |||||||
chr13:48405550 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+24107G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405550 | |||||||
chr13:48405687 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1695+24244A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405687 | |||||||
chr13:48405762 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+24319A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405762 | |||||||
chr13:48405777 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1695+24334C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405777 | |||||||
chr13:48405937 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1695+24494A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48405937 | |||||||
chr13:48406048 | AGGT | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1695+24609_1695+24 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48406048 | ||||||
chr13:48406098 | C | CTG | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.1695+24669_1695+24 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48406098 | ||||||
chr13:48406114 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1695+24671A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406114 | |||||||
chr13:48406126 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+24683A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406126 | |||||||
chr13:48406201 | ATG | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+24768_1695+24 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48406201 | ||||||
chr13:48406204 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1695+24761T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406204 | |||||||
chr13:48406679 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1695+25236G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406679 | |||||||
chr13:48406835 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1695+25392C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406835 | |||||||
chr13:48406894 | A | AAAAC | 25 | a0001c0001t0001g0109 a0001c0001t0001g0197 a0001c0001t0001g0200 others(22): Show |
25 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1695+25469_1695+25 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48406894 | ||||||
chr13:48406917 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1695+25474G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48406917 | |||||||
chr13:48407418 | A | C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | NA18980.hp1 NA19063.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+25975A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48407418 | |||||||
chr13:48407776 | G | A | 20 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1695+26333G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48407776 | |||||||
chr13:48408020 | T | C | 1 | a0001c0001t0001g0010 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1695+26577T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408020 | |||||||
chr13:48408070 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+26627C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408070 | |||||||
chr13:48408243 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+26800T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408243 | |||||||
chr13:48408251 | C | T | 7 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 others(4): Show |
8 | HG01192.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1695+26808C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408251 | |||||||
chr13:48408257 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1695+26814A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408257 | |||||||
chr13:48408660 | G | A | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1695+27217G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408660 | |||||||
chr13:48408837 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
298 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.1695+27394T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408837 | |||||||
chr13:48408916 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1695+27473T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48408916 | |||||||
chr13:48409029 | CAAAT | C | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+27590_1695+27 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409029 | ||||||
chr13:48409150 | C | CT | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1695+27723dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409150 | ||||||
chr13:48409152 | T | C | 2 | a0001c0001t0001g0296 a0005c0005t0001g0294 |
2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1695+27709T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48409152 | |||||||
chr13:48409570 | A | AT | 18 | a0001c0001t0001g0127 a0001c0001t0001g0205 a0001c0001t0001g0212 others(15): Show |
18 | HG01109.hp2 HG01361.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.1695+28156dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | A | ATT | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0224 others(5): Show |
8 | HG02257.hp1 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1695+28155_1695+28 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | AT | A | 25 | a0001c0001t0001g0048 a0001c0001t0001g0106 a0001c0001t0001g0111 others(22): Show |
25 | HG00099.hp1 HG01069.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1695+28156delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | ATT | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(33): Show |
36 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1695+28155_1695+28 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | ATTT | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
152 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1695+28154_1695+28 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | ATTTT | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG00738.hp1 HG01167.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1695+28153_1695+28 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409570 | ATTTTTTT others(4): Show |
A | 7 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 others(4): Show |
8 | HG01192.hp2 HG02055.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1695+28146_1695+28 others(17): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48409570 | ||||||
chr13:48409625 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1695+28182G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48409625 | |||||||
chr13:48409776 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(31): Show |
35 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1695+28333T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48409776 | |||||||
chr13:48409869 | G | A | 23 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1695+28426G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48409869 | |||||||
chr13:48409927 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1695+28484G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48409927 | |||||||
chr13:48410076 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1695+28633C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410076 | |||||||
chr13:48410184 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+28741C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410184 | |||||||
chr13:48410197 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1695+28754T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410197 | |||||||
chr13:48410199 | G | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1695+28756G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410199 | |||||||
chr13:48410481 | G | T | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1695+29038G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410481 | |||||||
chr13:48410586 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1695+29143G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410586 | |||||||
chr13:48410690 | T | G | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1695+29247T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410690 | |||||||
chr13:48410915 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1695+29472A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48410915 | |||||||
chr13:48411169 | C | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+29726C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48411169 | |||||||
chr13:48411303 | G | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0060 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1695+29860G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48411303 | |||||||
chr13:48411385 | T | C | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+29942T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48411385 | |||||||
chr13:48411436 | G | T | 1 | a0001c0001t0001g0271 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1695+29993G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48411436 | |||||||
chr13:48411839 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+30396A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48411839 | |||||||
chr13:48412278 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1695+30835C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48412278 | |||||||
chr13:48412591 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0168 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1695+31148G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48412591 | |||||||
chr13:48412614 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1695+31171C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48412614 | |||||||
chr13:48412896 | A | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1695+31453A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48412896 | |||||||
chr13:48413634 | C | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+32191C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48413634 | |||||||
chr13:48414006 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+32563C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414006 | |||||||
chr13:48414026 | A | G | 2 | a0001c0001t0006g0286 a0001c0001t0006g0287 |
2 | NA18998.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1695+32583A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414026 | |||||||
chr13:48414227 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1695+32784G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414227 | |||||||
chr13:48414262 | G | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+32819G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414262 | |||||||
chr13:48414342 | CA | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0118 others(44): Show |
49 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1695+32916delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48414342 | ||||||
chr13:48414394 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+32951G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414394 | |||||||
chr13:48414654 | CTT | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1695+33212_1695+33 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414654 | |||||||
chr13:48414776 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1695+33333A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414776 | |||||||
chr13:48414829 | G | C | 5 | a0001c0001t0001g0213 a0001c0001t0001g0220 a0001c0001t0001g0231 others(2): Show |
5 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695+33386G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414829 | |||||||
chr13:48414950 | C | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1695+33507C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48414950 | |||||||
chr13:48414993 | AT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1695+33560delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48414993 | ||||||
chr13:48415168 | A | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1695+33725A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415168 | |||||||
chr13:48415179 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1695+33736T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415179 | |||||||
chr13:48415190 | A | G | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1695+33747A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415190 | |||||||
chr13:48415383 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+33940A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415383 | |||||||
chr13:48415509 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+34066C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415509 | |||||||
chr13:48415665 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1695+34222A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415665 | |||||||
chr13:48415676 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1695+34233A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48415676 | |||||||
chr13:48416111 | C | T | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1695+34668C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416111 | |||||||
chr13:48416158 | A | G | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+34715A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416158 | |||||||
chr13:48416255 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(264): Show |
277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1695+34812C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416255 | |||||||
chr13:48416260 | A | AG | 42 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(39): Show |
44 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1695+34822dupG | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48416260 | ||||||
chr13:48416273 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1695+34830C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416273 | |||||||
chr13:48416282 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1695+34839C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416282 | |||||||
chr13:48416314 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00738.hp1 HG02055.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+34871C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416314 | |||||||
chr13:48416353 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1695+34910A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416353 | |||||||
chr13:48416415 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1695+34972T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416415 | |||||||
chr13:48416420 | G | A | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1695+34977G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416420 | |||||||
chr13:48416454 | T | C | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1695+35011T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416454 | |||||||
chr13:48416550 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1695+35107G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416550 | |||||||
chr13:48416606 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.1695+35163A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416606 | |||||||
chr13:48416818 | G | A | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+35375G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416818 | |||||||
chr13:48416899 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0058 others(2): Show |
5 | NA18943.hp2 NA18952.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.1695+35456A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416899 | |||||||
chr13:48416966 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1695+35523G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48416966 | |||||||
chr13:48417067 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1695+35624G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417067 | |||||||
chr13:48417168 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1695+35725C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417168 | |||||||
chr13:48417186 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1695+35743C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417186 | |||||||
chr13:48417187 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1695+35744G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417187 | |||||||
chr13:48417479 | C | T | 27 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(24): Show |
27 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1696-35514C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417479 | |||||||
chr13:48417480 | G | A | 8 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0077 others(5): Show |
8 | HG02818.hp2 HG03139.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1696-35513G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417480 | |||||||
chr13:48417694 | AC | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-35297delC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48417694 | ||||||
chr13:48417714 | A | G | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1696-35279A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417714 | |||||||
chr13:48417801 | A | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-35192A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417801 | |||||||
chr13:48417904 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1696-35089G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417904 | |||||||
chr13:48417978 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1696-35015T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417978 | |||||||
chr13:48417999 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-34994G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48417999 | |||||||
chr13:48418044 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-34949C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48418044 | |||||||
chr13:48418077 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1696-34916C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48418077 | |||||||
chr13:48418556 | C | T | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0282 |
3 | HG02129.hp1 NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1696-34437C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48418556 | |||||||
chr13:48418674 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
261 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.1696-34319G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48418674 | |||||||
chr13:48418709 | C | CA | 17 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0036 others(14): Show |
17 | HG00099.hp1 HG00558.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1696-34270dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48418709 | ||||||
chr13:48418709 | CA | C | 20 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-34270delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48418709 | ||||||
chr13:48419010 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0056 |
3 | HG00408.hp2 HG01496.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1696-33983C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419010 | |||||||
chr13:48419026 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1696-33967C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419026 | |||||||
chr13:48419126 | A | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-33867A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419126 | |||||||
chr13:48419247 | C | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-33746C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419247 | |||||||
chr13:48419337 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1696-33656A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419337 | |||||||
chr13:48419499 | A | G | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1696-33494A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419499 | |||||||
chr13:48419548 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1696-33445G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419548 | |||||||
chr13:48419551 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-33442G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419551 | |||||||
chr13:48419564 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1696-33429C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419564 | |||||||
chr13:48419847 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1696-33146G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419847 | |||||||
chr13:48419869 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-33124C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419869 | |||||||
chr13:48419887 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0077 |
2 | NA18987.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1696-33106C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419887 | |||||||
chr13:48419909 | C | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-33084C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419909 | |||||||
chr13:48419910 | A | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1696-33083A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419910 | |||||||
chr13:48419952 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1696-33041C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48419952 | |||||||
chr13:48420047 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-32946A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420047 | |||||||
chr13:48420199 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-32794G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420199 | |||||||
chr13:48420566 | G | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-32427G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420566 | |||||||
chr13:48420604 | T | C | 14 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1696-32389T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420604 | |||||||
chr13:48420744 | T | A | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-32249T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420744 | |||||||
chr13:48420747 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(31): Show |
35 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1696-32246A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420747 | |||||||
chr13:48420892 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1696-32101A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48420892 | |||||||
chr13:48421063 | C | T | 1 | a0001c0001t0004g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1696-31930C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421063 | |||||||
chr13:48421144 | C | G | 1 | a0001c0001t0002g0130 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1696-31849C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421144 | |||||||
chr13:48421261 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1696-31732A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421261 | |||||||
chr13:48421722 | C | G | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1696-31271C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421722 | |||||||
chr13:48421834 | G | A | 16 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(13): Show |
16 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1696-31159G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421834 | |||||||
chr13:48421916 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1696-31077G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421916 | |||||||
chr13:48421919 | G | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-31074G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48421919 | |||||||
chr13:48422017 | G | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-30976G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48422017 | |||||||
chr13:48422201 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1696-30792G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48422201 | |||||||
chr13:48422209 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-30784C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48422209 | |||||||
chr13:48422663 | T | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-30330T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48422663 | |||||||
chr13:48422792 | TA | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.1696-30191delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48422792 | ||||||
chr13:48423077 | C | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-29916C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423077 | |||||||
chr13:48423124 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-29869G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423124 | |||||||
chr13:48423305 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1696-29688T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423305 | |||||||
chr13:48423498 | C | A | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1696-29495C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423498 | |||||||
chr13:48423557 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0188 |
2 | HG00099.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1696-29436G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423557 | |||||||
chr13:48423617 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-29376C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423617 | |||||||
chr13:48423867 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1696-29126A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48423867 | |||||||
chr13:48424046 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-28947C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424046 | |||||||
chr13:48424146 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-28847C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424146 | |||||||
chr13:48424273 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-28720C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424273 | |||||||
chr13:48424277 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0156 a0001c0001t0001g0160 |
3 | HG01256.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1696-28716A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424277 | |||||||
chr13:48424345 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1696-28648G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424345 | |||||||
chr13:48424385 | A | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1696-28608A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424385 | |||||||
chr13:48424603 | C | CT | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-28383dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48424603 | ||||||
chr13:48424880 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(39): Show |
44 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1696-28113C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424880 | |||||||
chr13:48424895 | A | T | 1 | a0001c0001t0001g0097 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1696-28098A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48424895 | |||||||
chr13:48425210 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-27783A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425210 | |||||||
chr13:48425461 | G | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-27532G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425461 | |||||||
chr13:48425610 | C | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0053 others(1): Show |
4 | HG00733.hp2 HG00741.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-27383C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425610 | |||||||
chr13:48425611 | A | G | 10 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0001g0240 others(7): Show |
10 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1696-27382A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425611 | |||||||
chr13:48425621 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1696-27372G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425621 | |||||||
chr13:48425666 | A | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-27327A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425666 | |||||||
chr13:48425677 | T | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1696-27316T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425677 | |||||||
chr13:48425693 | G | GA | 17 | a0001c0001t0001g0043 a0001c0001t0001g0118 a0001c0001t0001g0119 others(14): Show |
17 | HG00099.hp1 HG00438.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1696-27290dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48425693 | ||||||
chr13:48425895 | G | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1696-27098G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425895 | |||||||
chr13:48425933 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1696-27060G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48425933 | |||||||
chr13:48426010 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0056 |
3 | HG00408.hp2 HG01496.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1696-26983A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426010 | |||||||
chr13:48426050 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1696-26943A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426050 | |||||||
chr13:48426140 | A | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-26853A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426140 | |||||||
chr13:48426298 | A | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(39): Show |
44 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1696-26695A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426298 | |||||||
chr13:48426561 | G | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-26432G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426561 | |||||||
chr13:48426766 | C | CT | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-26226dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48426766 | ||||||
chr13:48426888 | A | G | 2 | a0001c0001t0001g0296 a0005c0005t0001g0294 |
2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1696-26105A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426888 | |||||||
chr13:48426911 | T | A | 1 | a0001c0001t0001g0017 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1696-26082T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48426911 | |||||||
chr13:48427008 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1696-25985G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427008 | |||||||
chr13:48427121 | TTCTACCA others(43): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1696-25818_1696-25 others(56): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427121 | ||||||
chr13:48427145 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-25848T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427145 | |||||||
chr13:48427151 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-25842A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427151 | |||||||
chr13:48427165 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0183 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1696-25828C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427165 | |||||||
chr13:48427171 | ATCTACCA others(152): Show |
A | 17 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0202 others(14): Show |
17 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1696-25543_1696-25 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427171 | ||||||
chr13:48427186 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | NA18970.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1696-25807C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427186 | |||||||
chr13:48427195 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1696-25798T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427195 | |||||||
chr13:48427218 | G | A | 1 | a0001c0001t0007g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1696-25775G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427218 | |||||||
chr13:48427248 | T | C | 8 | a0001c0001t0001g0289 a0001c0001t0003g0004 a0001c0001t0003g0120 others(5): Show |
9 | HG01192.hp2 HG01975.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1696-25745T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427248 | |||||||
chr13:48427301 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-25692T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427301 | |||||||
chr13:48427313 | C | CTTCAACA others(46): Show |
1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1696-25628_1696-25 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427313 | ||||||
chr13:48427313 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1696-25680C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427313 | |||||||
chr13:48427366 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
222 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.1696-25627C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427366 | |||||||
chr13:48427397 | A | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0053 others(2): Show |
5 | HG00733.hp2 HG00741.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-25596A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427397 | |||||||
chr13:48427419 | C | T | 6 | a0001c0001t0001g0201 a0001c0001t0001g0247 a0001c0001t0005g0290 others(3): Show |
6 | HG01496.hp2 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1696-25574C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427419 | |||||||
chr13:48427450 | A | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0247 |
2 | HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1696-25543A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427450 | |||||||
chr13:48427452 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1696-25541C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427452 | |||||||
chr13:48427459 | A | ATTGGGGA others(47): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0165 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1696-25532_1696-25 others(60): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427459 | ||||||
chr13:48427472 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0247 |
2 | HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1696-25521C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427472 | |||||||
chr13:48427480 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1696-25513C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427480 | |||||||
chr13:48427505 | C | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
115 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1696-25488C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427505 | |||||||
chr13:48427513 | TTGGGGAG others(99): Show |
T | 1 | a0001c0001t0001g0247 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1696-25384_1696-25 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427513 | ||||||
chr13:48427513 | TTGGGGAG others(311): Show |
T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0053 others(1): Show |
4 | HG00733.hp2 HG00741.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-25427_1696-25 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427513 | ||||||
chr13:48427566 | T | C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0224 a0001c0001t0001g0225 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1696-25427T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427566 | |||||||
chr13:48427566 | TTGGGGAG others(46): Show |
T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(25): Show |
29 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1696-25384_1696-25 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427566 | ||||||
chr13:48427566 | TTGGGGAG others(205): Show |
T | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1696-25384_1696-25 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427566 | ||||||
chr13:48427578 | C | CTTCAACA others(46): Show |
30 | a0001c0001t0001g0044 a0001c0001t0001g0131 a0001c0001t0001g0132 others(27): Show |
30 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1696-25385_1696-25 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427578 | ||||||
chr13:48427578 | C | T | 20 | a0001c0001t0001g0035 a0001c0001t0001g0152 a0001c0001t0001g0165 others(17): Show |
20 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-25415C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427578 | |||||||
chr13:48427583 | A | ACACGAGT others(46): Show |
1 | a0001c0001t0007g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1696-25385_1696-25 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427583 | ||||||
chr13:48427609 | T | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
214 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1696-25384T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427609 | |||||||
chr13:48427619 | C | T | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1696-25374C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427619 | |||||||
chr13:48427631 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
193 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1696-25362C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427631 | |||||||
chr13:48427639 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1696-25354C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427639 | |||||||
chr13:48427662 | A | ACCTCCAG others(99): Show |
1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1696-25257_1696-25 others(112): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427662 | ||||||
chr13:48427662 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
212 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1696-25331A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427662 | |||||||
chr13:48427672 | T | C | 35 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(32): Show |
35 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.1696-25321T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427672 | |||||||
chr13:48427684 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(26): Show |
30 | HG00323.hp2 HG00673.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1696-25309C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427684 | |||||||
chr13:48427715 | A | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0016 others(25): Show |
29 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.1696-25278A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427715 | |||||||
chr13:48427725 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.1696-25268T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427725 | |||||||
chr13:48427725 | TTGGGGAG others(46): Show |
T | 1 | a0001c0001t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1696-25044_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427725 | ||||||
chr13:48427725 | TTGGGGAG others(99): Show |
T | 1 | a0001c0001t0001g0035 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1696-25097_1696-24 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427725 | ||||||
chr13:48427725 | TTGGGGAG others(205): Show |
T | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1696-25203_1696-24 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427725 | ||||||
chr13:48427778 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
231 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.1696-25215C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427778 | |||||||
chr13:48427787 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1696-25206A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427787 | |||||||
chr13:48427820 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(14): Show |
17 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1696-25173C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427820 | |||||||
chr13:48427831 | C | T | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(48): Show |
52 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1696-25162C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427831 | |||||||
chr13:48427873 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0086 others(4): Show |
7 | HG00673.hp1 HG01255.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-25120C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427873 | |||||||
chr13:48427884 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0285 |
2 | HG00323.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1696-25109C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427884 | |||||||
chr13:48427896 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
81 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1696-25097C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427896 | |||||||
chr13:48427904 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1696-25089C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427904 | |||||||
chr13:48427937 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(78): Show |
81 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1696-25056C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427937 | |||||||
chr13:48427949 | C | T | 153 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
153 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1696-25044C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427949 | |||||||
chr13:48427990 | C | CTGGGGAG others(152): Show |
1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1696-24992_1696-24 others(165): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427990 | ||||||
chr13:48427990 | C | CTGGGGAG others(152): Show |
1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1696-24992_1696-24 others(165): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427990 | ||||||
chr13:48427990 | C | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0016 others(67): Show |
70 | HG00558.hp1 HG00673.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.1696-25003C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427990 | |||||||
chr13:48427990 | CTGGGGAG others(46): Show |
C | 27 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(24): Show |
28 | HG02129.hp1 HG02155.hp1 HG02165.hp1 others(25): Show |
intron_variant | MODIFIER | c.1696-24572_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427990 | ||||||
chr13:48427990 | CTGGGGAG others(46): Show |
T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
83 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1696-25003_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427990 | |||||||
chr13:48427990 | CTGGGGAG others(99): Show |
T | 1 | a0001c0001t0001g0075 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1696-25003_1696-24 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48427990 | |||||||
chr13:48427990 | CTGGGGAG others(205): Show |
C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1696-24731_1696-24 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48427990 | ||||||
chr13:48428002 | T | C | 37 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(34): Show |
38 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.1696-24991T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428002 | |||||||
chr13:48428039 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1696-24954A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428039 | |||||||
chr13:48428043 | T | C | 35 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(32): Show |
35 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.1696-24950T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428043 | |||||||
chr13:48428055 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-24938T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428055 | |||||||
chr13:48428092 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1696-24901A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428092 | |||||||
chr13:48428096 | T | TTGGGGAG others(205): Show |
4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-24833_1696-24 others(218): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48428096 | ||||||
chr13:48428119 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1696-24874G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428119 | |||||||
chr13:48428183 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1696-24810C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428183 | |||||||
chr13:48428214 | T | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1696-24779T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428214 | |||||||
chr13:48428255 | T | C | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1696-24738T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428255 | |||||||
chr13:48428275 | C | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1696-24718C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428275 | |||||||
chr13:48428368 | G | GCACATTT others(46): Show |
1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1696-24573_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48428368 | ||||||
chr13:48428390 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1696-24603T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428390 | |||||||
chr13:48428421 | G | GCACATTT others(46): Show |
57 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0044 others(54): Show |
62 | HG00408.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.1696-24555_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48428421 | ||||||
chr13:48428421 | G | T | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1696-24572G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428421 | |||||||
chr13:48428453 | C | CCTCACCT others(46): Show |
4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-24503_1696-24 others(59): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48428453 | ||||||
chr13:48428474 | T | G | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1696-24519T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428474 | |||||||
chr13:48428722 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-24271A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48428722 | |||||||
chr13:48429103 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-23890A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429103 | |||||||
chr13:48429319 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1696-23674G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429319 | |||||||
chr13:48429619 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-23374G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429619 | |||||||
chr13:48429642 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0220 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1696-23351C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429642 | |||||||
chr13:48429776 | A | C | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-23217A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429776 | |||||||
chr13:48429996 | A | G | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1696-22997A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48429996 | |||||||
chr13:48430212 | C | G | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1696-22781C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430212 | |||||||
chr13:48430233 | A | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | NA18961.hp1 NA18972.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1696-22760A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430233 | |||||||
chr13:48430469 | T | C | 1 | a0001c0001t0007g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1696-22524T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430469 | |||||||
chr13:48430611 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1696-22382G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430611 | |||||||
chr13:48430632 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 |
3 | HG02257.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1696-22361C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430632 | |||||||
chr13:48430749 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-22244A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430749 | |||||||
chr13:48430765 | CA | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
226 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1696-22216delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48430765 | ||||||
chr13:48430769 | A | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(35): Show |
39 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1696-22224A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430769 | |||||||
chr13:48430770 | A | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(189): Show |
200 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1696-22223A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430770 | |||||||
chr13:48430774 | A | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0168 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1696-22219A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48430774 | |||||||
chr13:48431096 | T | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-21897T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431096 | |||||||
chr13:48431123 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-21870G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431123 | |||||||
chr13:48431142 | CA | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1696-21845delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48431142 | ||||||
chr13:48431248 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-21745A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431248 | |||||||
chr13:48431379 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1696-21614C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431379 | |||||||
chr13:48431411 | A | G | 1 | a0001c0001t0005g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1696-21582A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431411 | |||||||
chr13:48431740 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1696-21253G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48431740 | |||||||
chr13:48432129 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-20864G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432129 | |||||||
chr13:48432349 | G | A | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1696-20644G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432349 | |||||||
chr13:48432350 | T | A | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1696-20643T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432350 | |||||||
chr13:48432363 | T | TTCTGCTT others(296): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-20614_1696-20 others(309): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48432363 | ||||||
chr13:48432427 | G | GT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0244 a0001c0001t0001g0259 others(28): Show |
32 | HG00323.hp2 HG01109.hp2 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.1696-20555dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48432427 | ||||||
chr13:48432475 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1696-20518C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432475 | |||||||
chr13:48432499 | A | G | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-20494A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432499 | |||||||
chr13:48432823 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1696-20170G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48432823 | |||||||
chr13:48433147 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1696-19846G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433147 | |||||||
chr13:48433283 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1696-19710T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433283 | |||||||
chr13:48433399 | C | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-19594C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433399 | |||||||
chr13:48433404 | TGAA | T | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-19583_1696-19 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48433404 | ||||||
chr13:48433503 | A | C | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1696-19490A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433503 | |||||||
chr13:48433533 | T | C | 4 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-19460T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433533 | |||||||
chr13:48433599 | C | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0218 a0001c0001t0001g0219 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1696-19394C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433599 | |||||||
chr13:48433621 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-19372A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433621 | |||||||
chr13:48433655 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-19338T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433655 | |||||||
chr13:48433682 | A | AT | 42 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0067 others(39): Show |
43 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1696-19298dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48433682 | ||||||
chr13:48433682 | A | ATT | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1696-19299_1696-19 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48433682 | ||||||
chr13:48433747 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1696-19246C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433747 | |||||||
chr13:48433927 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0061 a0001c0001t0001g0067 others(1): Show |
4 | HG00673.hp2 NA18980.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-19066T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48433927 | |||||||
chr13:48434121 | T | C | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-18872T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434121 | |||||||
chr13:48434281 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-18712C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434281 | |||||||
chr13:48434538 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1696-18455A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434538 | |||||||
chr13:48434584 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-18409T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434584 | |||||||
chr13:48434702 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0151 |
5 | NA18971.hp2 NA18977.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-18291C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434702 | |||||||
chr13:48434731 | T | G | 1 | a0001c0001t0001g0269 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1696-18262T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48434731 | |||||||
chr13:48435097 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-17896G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435097 | |||||||
chr13:48435174 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1696-17819G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435174 | |||||||
chr13:48435573 | T | A | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1696-17420T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435573 | |||||||
chr13:48435576 | A | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-17417A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435576 | |||||||
chr13:48435599 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1696-17394T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435599 | |||||||
chr13:48435610 | T | C | 1 | a0001c0004t0001g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1696-17383T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435610 | |||||||
chr13:48435778 | A | G | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1696-17215A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435778 | |||||||
chr13:48435803 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-17190A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435803 | |||||||
chr13:48435917 | C | T | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1696-17076C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48435917 | |||||||
chr13:48436034 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-16959G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436034 | |||||||
chr13:48436206 | T | C | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-16787T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436206 | |||||||
chr13:48436349 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-16644T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436349 | |||||||
chr13:48436366 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-16627A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436366 | |||||||
chr13:48436535 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-16458C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436535 | |||||||
chr13:48436571 | A | C | 1 | a0001c0001t0001g0012 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1696-16422A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436571 | |||||||
chr13:48436603 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-16390A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436603 | |||||||
chr13:48436611 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1696-16382C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436611 | |||||||
chr13:48436643 | TA | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-16339delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48436643 | ||||||
chr13:48436951 | A | G | 34 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(31): Show |
35 | HG01109.hp2 HG01192.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1696-16042A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48436951 | |||||||
chr13:48437216 | A | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1696-15777A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437216 | |||||||
chr13:48437414 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-15579A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437414 | |||||||
chr13:48437444 | A | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
278 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.1696-15549A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437444 | |||||||
chr13:48437468 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-15525G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437468 | |||||||
chr13:48437472 | C | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-15521C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437472 | |||||||
chr13:48437478 | T | G | 1 | a0001c0001t0001g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1696-15515T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437478 | |||||||
chr13:48437549 | G | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02145.hp1 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-15444G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437549 | |||||||
chr13:48437786 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1696-15207C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437786 | |||||||
chr13:48437829 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1696-15164A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48437829 | |||||||
chr13:48438005 | T | C | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-14988T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438005 | |||||||
chr13:48438074 | A | G | 4 | a0002c0002t0001g0250 a0002c0002t0001g0251 a0002c0002t0001g0252 others(1): Show |
4 | HG02818.hp2 HG03225.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-14919A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438074 | |||||||
chr13:48438129 | G | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1696-14864G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438129 | |||||||
chr13:48438299 | A | G | 26 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(23): Show |
27 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1696-14694A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438299 | |||||||
chr13:48438312 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1696-14681A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438312 | |||||||
chr13:48438352 | C | G | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1696-14641C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438352 | |||||||
chr13:48438357 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
194 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1696-14636G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438357 | |||||||
chr13:48438707 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-14286G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438707 | |||||||
chr13:48438809 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1696-14184G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438809 | |||||||
chr13:48438899 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-14094C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48438899 | |||||||
chr13:48438936 | TTCTCTTA others(3): Show |
T | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1696-14051_1696-14 others(16): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48438936 | ||||||
chr13:48439092 | C | CTAGTATG others(4): Show |
1 | a0001c0001t0001g0276 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1696-13901_1696-13 others(17): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439092 | |||||||
chr13:48439093 | G | C | 1 | a0001c0001t0001g0276 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1696-13900G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439093 | |||||||
chr13:48439121 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1696-13872C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439121 | |||||||
chr13:48439371 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-13622A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439371 | |||||||
chr13:48439588 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(253): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1696-13405C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439588 | |||||||
chr13:48439610 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-13383G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439610 | |||||||
chr13:48439675 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-13318G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439675 | |||||||
chr13:48439761 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02145.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1696-13232G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48439761 | |||||||
chr13:48440015 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-12978G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440015 | |||||||
chr13:48440030 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1696-12963T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440030 | |||||||
chr13:48440285 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1696-12708C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440285 | |||||||
chr13:48440366 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1696-12627G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440366 | |||||||
chr13:48440442 | C | A | 7 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1696-12551C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440442 | |||||||
chr13:48440602 | G | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0133 a0001c0001t0001g0136 others(6): Show |
12 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1696-12391G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440602 | |||||||
chr13:48440697 | G | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-12296G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440697 | |||||||
chr13:48440793 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1696-12200A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48440793 | |||||||
chr13:48441159 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1696-11834A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441159 | |||||||
chr13:48441274 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1696-11719A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441274 | |||||||
chr13:48441356 | G | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1696-11637G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441356 | |||||||
chr13:48441701 | G | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1696-11292G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441701 | |||||||
chr13:48441751 | TATATATA others(21): Show |
T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-11239_1696-11 others(34): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48441751 | ||||||
chr13:48441820 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-11173A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441820 | |||||||
chr13:48441927 | T | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1696-11066T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48441927 | |||||||
chr13:48442206 | AT | A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0197 a0001c0001t0001g0200 others(17): Show |
20 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-10775delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48442206 | ||||||
chr13:48442211 | T | A | 5 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-10782T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442211 | |||||||
chr13:48442320 | C | A | 1 | a0004c0006t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1696-10673C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442320 | |||||||
chr13:48442326 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-10667G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442326 | |||||||
chr13:48442362 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(221): Show |
233 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.1696-10631G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442362 | |||||||
chr13:48442374 | G | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1696-10619G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442374 | |||||||
chr13:48442508 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-10485C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442508 | |||||||
chr13:48442811 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-10182C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48442811 | |||||||
chr13:48443251 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0220 |
2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1696-9742T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443251 | |||||||
chr13:48443255 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1696-9738A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443255 | |||||||
chr13:48443298 | T | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-9695T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443298 | |||||||
chr13:48443433 | CA | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(32): Show |
36 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1696-9554delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48443433 | ||||||
chr13:48443480 | A | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-9513A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443480 | |||||||
chr13:48443903 | G | A | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1696-9090G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443903 | |||||||
chr13:48443929 | T | C | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-9064T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443929 | |||||||
chr13:48443994 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1696-8999T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48443994 | |||||||
chr13:48444117 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1696-8876C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444117 | |||||||
chr13:48444234 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1696-8759A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444234 | |||||||
chr13:48444346 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1696-8647G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444346 | |||||||
chr13:48444554 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1696-8439G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444554 | |||||||
chr13:48444603 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-8390G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444603 | |||||||
chr13:48444629 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1696-8364A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444629 | |||||||
chr13:48444646 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1696-8347G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444646 | |||||||
chr13:48444649 | G | A | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-8344G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444649 | |||||||
chr13:48444848 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1696-8145G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48444848 | |||||||
chr13:48444988 | GT | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.1696-7992delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48444988 | ||||||
chr13:48444988 | GTT | G | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(108): Show |
111 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1696-7993_1696-799 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48444988 | ||||||
chr13:48445058 | G | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(32): Show |
36 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1696-7935G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445058 | |||||||
chr13:48445113 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1696-7880G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445113 | |||||||
chr13:48445253 | A | G | 14 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1696-7740A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445253 | |||||||
chr13:48445280 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1696-7713T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445280 | |||||||
chr13:48445534 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1696-7459T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445534 | |||||||
chr13:48445589 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1696-7404A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445589 | |||||||
chr13:48445599 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
198 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1696-7394G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445599 | |||||||
chr13:48445615 | C | T | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1696-7378C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445615 | |||||||
chr13:48445774 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1696-7219G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445774 | |||||||
chr13:48445953 | G | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-7040G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48445953 | |||||||
chr13:48446020 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1696-6973C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446020 | |||||||
chr13:48446031 | C | G | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1696-6962C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446031 | |||||||
chr13:48446388 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1696-6605C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446388 | |||||||
chr13:48446497 | T | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1696-6496T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446497 | |||||||
chr13:48446656 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02647.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1696-6337G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446656 | |||||||
chr13:48446765 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1696-6228C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446765 | |||||||
chr13:48446876 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1696-6117C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446876 | |||||||
chr13:48446909 | G | A | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1696-6084G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446909 | |||||||
chr13:48446949 | A | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0279 |
2 | HG02165.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1696-6044A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48446949 | |||||||
chr13:48447234 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1696-5759C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48447234 | |||||||
chr13:48447384 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1696-5609T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48447384 | |||||||
chr13:48447656 | A | AT | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-5335dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48447656 | ||||||
chr13:48447750 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1696-5243G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48447750 | |||||||
chr13:48447883 | C | A | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696-5110C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48447883 | |||||||
chr13:48448200 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-4793G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448200 | |||||||
chr13:48448395 | C | T | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-4598C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448395 | |||||||
chr13:48448634 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1696-4359A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448634 | |||||||
chr13:48448637 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1696-4356A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448637 | |||||||
chr13:48448658 | G | T | 23 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1696-4335G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448658 | |||||||
chr13:48448706 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0105 a0001c0001t0001g0107 |
3 | NA18950.hp1 NA18990.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1696-4287A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448706 | |||||||
chr13:48448768 | T | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-4225T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448768 | |||||||
chr13:48448784 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1696-4209C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448784 | |||||||
chr13:48448813 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-4180A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448813 | |||||||
chr13:48448891 | T | A | 1 | a0001c0001t0001g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1696-4102T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448891 | |||||||
chr13:48448892 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1696-4101G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48448892 | |||||||
chr13:48449109 | G | GT | 8 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0268 others(5): Show |
8 | HG01243.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1696-3875dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48449109 | ||||||
chr13:48449146 | A | G | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-3847A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449146 | |||||||
chr13:48449298 | A | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0086 a0001c0001t0001g0087 others(11): Show |
14 | HG00673.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1696-3695A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449298 | |||||||
chr13:48449351 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1696-3642G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449351 | |||||||
chr13:48449562 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | NA18906.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1696-3431A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449562 | |||||||
chr13:48449631 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0196 |
2 | HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1696-3362G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449631 | |||||||
chr13:48449977 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1696-3016T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48449977 | |||||||
chr13:48450091 | TA | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0125 others(3): Show |
6 | HG02486.hp1 HG02723.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1696-2901delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450091 | |||||||
chr13:48450092 | A | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1696-2901A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450092 | |||||||
chr13:48450093 | TA | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(31): Show |
34 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1696-2899delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450093 | |||||||
chr13:48450094 | A | AT | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(42): Show |
53 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1696-2886dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48450094 | ||||||
chr13:48450094 | A | T | 41 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(38): Show |
41 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1696-2899A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450094 | |||||||
chr13:48450094 | AT | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0028 others(42): Show |
46 | HG00099.hp1 HG00323.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.1696-2886delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48450094 | ||||||
chr13:48450095 | T | TA | 35 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0178 others(32): Show |
36 | HG00558.hp2 HG00738.hp2 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.1696-2898_1696-289 others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450095 | |||||||
chr13:48450096 | T | A | 9 | a0001c0001t0001g0046 a0001c0001t0001g0102 a0001c0001t0001g0257 others(6): Show |
9 | HG01109.hp2 HG02630.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1696-2897T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450096 | |||||||
chr13:48450097 | T | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(31): Show |
36 | HG00323.hp2 HG00558.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.1696-2896T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450097 | |||||||
chr13:48450098 | T | A | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1696-2895T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450098 | |||||||
chr13:48450415 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1696-2578G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450415 | |||||||
chr13:48450514 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-2479C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450514 | |||||||
chr13:48450580 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1696-2413T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450580 | |||||||
chr13:48450644 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-2349C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450644 | |||||||
chr13:48450777 | G | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.1696-2216G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450777 | |||||||
chr13:48450812 | A | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0131 a0001c0001t0001g0174 |
3 | HG00741.hp1 HG01975.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1696-2181A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450812 | |||||||
chr13:48450840 | G | A | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-2153G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450840 | |||||||
chr13:48450978 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1696-2015T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48450978 | |||||||
chr13:48451271 | T | G | 1 | a0001c0001t0001g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1696-1722T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451271 | |||||||
chr13:48451532 | T | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-1461T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451532 | |||||||
chr13:48451627 | G | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1696-1366G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451627 | |||||||
chr13:48451738 | AT | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1696-1239delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr13 | 48451738 | ||||||
chr13:48451787 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1696-1206C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451787 | |||||||
chr13:48451802 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1696-1191G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451802 | |||||||
chr13:48451997 | C | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-996C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48451997 | |||||||
chr13:48452116 | G | T | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1696-877G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452116 | |||||||
chr13:48452240 | A | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1696-753A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452240 | |||||||
chr13:48452385 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1696-608C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452385 | |||||||
chr13:48452716 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1696-277C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452716 | |||||||
chr13:48452779 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1696-214T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452779 | |||||||
chr13:48452821 | T | C | 1 | a0001c0001t0004g0238 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1696-172T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452821 | |||||||
chr13:48452839 | G | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1696-154G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 17/26 | chr13 | 48452839 | |||||||
chr13:48453367 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1814+256G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48453367 | |||||||
chr13:48453450 | C | G | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1814+339C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48453450 | |||||||
chr13:48453505 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1814+394G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48453505 | |||||||
chr13:48453779 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1814+668G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48453779 | |||||||
chr13:48454000 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+889A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48454000 | |||||||
chr13:48454104 | G | A | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1814+993G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48454104 | |||||||
chr13:48454214 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1814+1103C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48454214 | |||||||
chr13:48454708 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815-1496C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48454708 | |||||||
chr13:48455148 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1815-1056A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455148 | |||||||
chr13:48455249 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1815-955T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455249 | |||||||
chr13:48455303 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1815-901C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455303 | |||||||
chr13:48455529 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1815-675A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455529 | |||||||
chr13:48455653 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1815-551C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455653 | |||||||
chr13:48455750 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1815-454G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48455750 | |||||||
chr13:48456091 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1815-113A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48456091 | |||||||
chr13:48456100 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(31): Show |
35 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1815-104A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48456100 | |||||||
chr13:48456147 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1815-57A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 18/26 | chr13 | 48456147 | |||||||
chr13:48456506 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1960+157C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456506 | |||||||
chr13:48456566 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1960+217C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456566 | |||||||
chr13:48456659 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1960+310A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456659 | |||||||
chr13:48456707 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0079 |
2 | NA19004.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1960+358C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456707 | |||||||
chr13:48456835 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1960+486G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456835 | |||||||
chr13:48456926 | C | A | 23 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1960+577C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48456926 | |||||||
chr13:48457215 | A | C | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1960+866A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457215 | |||||||
chr13:48457401 | G | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(186): Show |
197 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1960+1052G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457401 | |||||||
chr13:48457430 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0228 a0001c0001t0001g0229 |
3 | HG00738.hp2 HG01168.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1960+1081C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457430 | |||||||
chr13:48457447 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1960+1098C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457447 | |||||||
chr13:48457559 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1960+1210G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457559 | |||||||
chr13:48457666 | C | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1960+1317C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457666 | |||||||
chr13:48457684 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1960+1335T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457684 | |||||||
chr13:48457686 | C | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0048 |
2 | HG01361.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1960+1337C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457686 | |||||||
chr13:48457692 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1960+1343C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457692 | |||||||
chr13:48457696 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(105): Show |
108 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1960+1347C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457696 | |||||||
chr13:48457765 | G | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0007t0001g0207 |
3 | HG02145.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1960+1416G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457765 | |||||||
chr13:48457820 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1960+1471C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457820 | |||||||
chr13:48457886 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0254 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1960+1537C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457886 | |||||||
chr13:48457995 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1960+1646C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48457995 | |||||||
chr13:48458128 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0185 |
2 | NA19005.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1961-1560T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458128 | |||||||
chr13:48458293 | G | GTA | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
302 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1961-1389_1961-138 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr13 | 48458293 | ||||||
chr13:48458308 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG04115.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1961-1380T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458308 | |||||||
chr13:48458335 | A | C | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1961-1353A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458335 | |||||||
chr13:48458538 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1961-1150T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458538 | |||||||
chr13:48458648 | G | A | 2 | a0001c0001t0003g0004 a0001c0001t0003g0121 |
3 | HG01192.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1961-1040G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458648 | |||||||
chr13:48458651 | G | T | 10 | a0001c0001t0001g0197 a0001c0001t0001g0234 a0001c0001t0001g0235 others(7): Show |
10 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1961-1037G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458651 | |||||||
chr13:48458868 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961-820A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458868 | |||||||
chr13:48458913 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1961-775T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458913 | |||||||
chr13:48458992 | A | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961-696A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48458992 | |||||||
chr13:48459038 | TG | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1961-648delG | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | INFO_REALIGN_3_PRIME | chr13 | 48459038 | ||||||
chr13:48459112 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1961-576C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48459112 | |||||||
chr13:48459326 | A | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1961-362A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48459326 | |||||||
chr13:48459414 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1961-274T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48459414 | |||||||
chr13:48459532 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1961-156T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48459532 | |||||||
chr13:48459611 | G | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1961-77G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 19/26 | chr13 | 48459611 | |||||||
chr13:48459886 | A | AT | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.2106+55dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCT | 5 | a0001c0001t0001g0212 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG02970.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+116_2106+119d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCTTTC others(1): Show |
6 | a0001c0001t0001g0209 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG02559.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+112_2106+119d others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCTTTC others(5): Show |
3 | a0001c0001t0001g0219 a0001c0001t0001g0228 a0001c0001t0001g0232 |
3 | HG00738.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2106+108_2106+119d others(14): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCTTTC others(9): Show |
2 | a0001c0001t0001g0215 a0001c0001t0001g0229 |
2 | HG01168.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2106+104_2106+119d others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCTTTC others(13): Show |
1 | a0001c0001t0001g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2106+100_2106+119d others(22): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTCTTTC others(21): Show |
1 | a0001c0001t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2106+92_2106+119du others(29): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTATTT others(10): Show |
2 | a0001c0001t0001g0081 a0001c0004t0001g0074 |
2 | NA19065.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(17): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTCT | 33 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0023 others(30): Show |
33 | HG00323.hp1 HG00438.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTCTTT others(2): Show |
16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(13): Show |
16 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTCTTT others(6): Show |
7 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0036 others(4): Show |
7 | HG03942.hp2 HG04204.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(13): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTCTTT others(10): Show |
4 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0001t0001g0058 others(1): Show |
4 | HG00558.hp1 NA18970.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(17): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | ATTTCTTT others(11): Show |
1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2106+55_2106+56ins others(18): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | A | C | 8 | a0001c0001t0001g0235 a0001c0001t0001g0275 a0001c0001t0001g0278 others(5): Show |
8 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2106+53A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459886 | |||||||
chr13:48459886 | ATTC | A | 15 | a0001c0001t0001g0163 a0001c0001t0001g0197 a0001c0001t0001g0203 others(12): Show |
16 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2106+56_2106+58del others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | ATTCT | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0216 a0001c0001t0001g0225 others(2): Show |
5 | HG02257.hp1 HG02818.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2106+116_2106+119d others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | ATTCTTTC | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0192 a0001c0001t0001g0200 |
3 | HG02145.hp2 HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2106+56_2106+62del others(7): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459886 | ATTCTTTC others(8): Show |
A | 1 | a0004c0006t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2106+56_2106+70del others(15): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459886 | ||||||
chr13:48459888 | T | TTC | 5 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(2): Show |
5 | HG01109.hp2 HG02630.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+55_2106+56ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459888 | |||||||
chr13:48459888 | T | TTCTTTTC others(588): Show |
1 | a0001c0001t0001g0235 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2106+55_2106+56ins others(595): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459888 | |||||||
chr13:48459888 | T | TTCTTTTC others(87): Show |
1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2106+55_2106+56ins others(94): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459888 | |||||||
chr13:48459888 | T | TTCTTTTC others(402): Show |
1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2106+55_2106+56ins others(409): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459888 | |||||||
chr13:48459889 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2106+56C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459889 | |||||||
chr13:48459889 | C | T | 7 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0004g0237 others(4): Show |
7 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2106+56C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459889 | |||||||
chr13:48459893 | C | CT | 8 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0239 others(5): Show |
8 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2106+63dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459893 | ||||||
chr13:48459894 | TTTC | T | 6 | a0001c0001t0001g0206 a0001c0001t0001g0241 a0001c0001t0001g0255 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+64_2106+66del others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459894 | ||||||
chr13:48459895 | T | C | 1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2106+62T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459895 | |||||||
chr13:48459896 | T | C | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2106+63T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459896 | |||||||
chr13:48459896 | T | TTC | 6 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0004g0237 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+63_2106+64ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459896 | |||||||
chr13:48459897 | C | T | 8 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 others(5): Show |
8 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2106+64C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459897 | |||||||
chr13:48459898 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+65T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459898 | |||||||
chr13:48459898 | TTTC | T | 11 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
12 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2106+68_2106+70del others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459898 | ||||||
chr13:48459900 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2106+67T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459900 | |||||||
chr13:48459901 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0275 a0001c0001t0008g0274 |
3 | HG02970.hp1 HG03098.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2106+68C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459901 | |||||||
chr13:48459904 | T | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(8): Show |
11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2106+71T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459904 | |||||||
chr13:48459904 | T | TTC | 6 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0004g0237 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+71_2106+72ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459904 | |||||||
chr13:48459905 | C | T | 6 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0004g0237 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+72C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459905 | |||||||
chr13:48459906 | T | TTTCCTTC others(29): Show |
1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2106+76_2106+77ins others(36): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(37): Show |
2 | a0001c0001t0001g0273 a0001c0001t0001g0277 |
2 | NA18979.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2106+76_2106+77ins others(44): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(41): Show |
1 | a0001c0001t0001g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2106+76_2106+77ins others(48): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(45): Show |
4 | a0001c0001t0001g0266 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG00323.hp2 NA18939.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+76_2106+77ins others(52): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(49): Show |
8 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0264 others(5): Show |
8 | HG03669.hp2 NA18944.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.2106+76_2106+77ins others(56): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(53): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0265 a0001c0001t0001g0276 others(3): Show |
7 | HG02165.hp1 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.2106+76_2106+77ins others(60): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(57): Show |
2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18956.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2106+76_2106+77ins others(64): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459906 | T | TTTCCTTC others(61): Show |
1 | a0001c0001t0001g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2106+76_2106+77ins others(68): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459906 | ||||||
chr13:48459908 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+75T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459908 | |||||||
chr13:48459909 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0275 a0001c0001t0008g0274 |
3 | HG02970.hp1 HG03098.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2106+76C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459909 | |||||||
chr13:48459910 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0259 others(23): Show |
27 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.2106+77T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459910 | |||||||
chr13:48459912 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+79T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459912 | |||||||
chr13:48459912 | T | TTC | 4 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0004g0238 others(1): Show |
4 | HG00558.hp2 HG02630.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+79_2106+80ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459912 | |||||||
chr13:48459912 | T | TTCTTTTC others(310): Show |
1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2106+79_2106+80ins others(317): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459912 | |||||||
chr13:48459913 | C | T | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 others(4): Show |
7 | HG00558.hp2 HG02630.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.2106+80C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459913 | |||||||
chr13:48459914 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(23): Show |
27 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.2106+81T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459914 | |||||||
chr13:48459914 | T | TTTCCTTC others(137): Show |
1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2106+84_2106+85ins others(144): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459914 | ||||||
chr13:48459915 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+82T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459915 | |||||||
chr13:48459916 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+83T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459916 | |||||||
chr13:48459917 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0275 a0001c0001t0004g0237 |
3 | HG03098.hp1 NA18995.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2106+84C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459917 | |||||||
chr13:48459918 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2106+85T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459918 | |||||||
chr13:48459919 | T | C | 1 | a0001c0001t0004g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2106+86T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459919 | |||||||
chr13:48459920 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2106+87T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459920 | |||||||
chr13:48459920 | T | TTC | 3 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2106+87_2106+88ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459920 | |||||||
chr13:48459921 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 others(1): Show |
4 | HG00558.hp2 HG02970.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+88C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459921 | |||||||
chr13:48459922 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(23): Show |
27 | HG00099.hp1 HG00323.hp2 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.2106+89T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459922 | |||||||
chr13:48459923 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+90_2106+91ins others(1): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459923 | |||||||
chr13:48459924 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+91T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459924 | |||||||
chr13:48459926 | T | C | 18 | a0001c0001t0001g0005 a0001c0001t0001g0261 a0001c0001t0001g0262 others(15): Show |
19 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.2106+93T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459926 | |||||||
chr13:48459926 | T | TTTCCTTC others(105): Show |
1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2106+96_2106+97ins others(112): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459926 | ||||||
chr13:48459927 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+94_2106+95ins others(1): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459927 | |||||||
chr13:48459927 | TTCTTTCT others(45): Show |
T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+96_2106+147de others(53): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459927 | ||||||
chr13:48459928 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+95T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459928 | |||||||
chr13:48459928 | T | TTC | 3 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2106+95_2106+96ins others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459928 | |||||||
chr13:48459929 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 others(1): Show |
4 | HG00558.hp2 HG02970.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+96C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459929 | |||||||
chr13:48459930 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+97T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459930 | |||||||
chr13:48459931 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+98_2106+99ins others(1): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459931 | |||||||
chr13:48459932 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+99T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459932 | |||||||
chr13:48459933 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+100C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459933 | |||||||
chr13:48459934 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2106+101T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459934 | |||||||
chr13:48459935 | T | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+102T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459935 | |||||||
chr13:48459935 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+102_2106+103i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459935 | |||||||
chr13:48459936 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+103T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459936 | |||||||
chr13:48459936 | T | TTC | 3 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2106+103_2106+104i others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459936 | |||||||
chr13:48459937 | C | T | 4 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0278 others(1): Show |
4 | HG00558.hp2 HG02970.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+104C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459937 | |||||||
chr13:48459938 | TTTC | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0116 others(7): Show |
10 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2106+108_2106+110d others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459938 | ||||||
chr13:48459939 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+106_2106+107i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459939 | |||||||
chr13:48459940 | T | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2106+107T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459940 | |||||||
chr13:48459941 | C | CT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(17): Show |
20 | HG00741.hp2 HG01169.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.2106+111dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459941 | ||||||
chr13:48459941 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+108C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459941 | |||||||
chr13:48459943 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+110_2106+111i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459943 | |||||||
chr13:48459944 | T | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2106+111T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459944 | |||||||
chr13:48459944 | T | TTC | 3 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2106+111_2106+112i others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459944 | |||||||
chr13:48459945 | C | T | 3 | a0001c0001t0001g0235 a0001c0001t0001g0278 a0001c0001t0008g0274 |
3 | HG00558.hp2 HG02970.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2106+112C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459945 | |||||||
chr13:48459947 | T | TC | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+114_2106+115i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459947 | |||||||
chr13:48459947 | TTCTTTTT others(25): Show |
T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2106+116_2106+147d others(34): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459947 | ||||||
chr13:48459948 | T | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG02965.hp2 HG02976.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2106+115T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459948 | |||||||
chr13:48459949 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
34 | HG00609.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.2106+116C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459949 | |||||||
chr13:48459949 | CT | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(29): Show |
33 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.2106+121delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459949 | ||||||
chr13:48459949 | CTT | C | 13 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2106+120_2106+121d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459949 | ||||||
chr13:48459950 | T | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
34 | HG00609.hp2 HG01167.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.2106+117T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459950 | |||||||
chr13:48459950 | T | TTTC | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2106+119_2106+120i others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459950 | ||||||
chr13:48459951 | T | TCCTTCCT others(3): Show |
1 | a0001c0001t0001g0127 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2106+118_2106+119i others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459951 | |||||||
chr13:48459951 | T | TTC | 38 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0049 others(35): Show |
39 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2106+119_2106+120i others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459951 | ||||||
chr13:48459951 | T | TTCTTTCC others(222): Show |
1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2106+119_2106+120i others(231): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459951 | ||||||
chr13:48459951 | T | TTCTTTCT others(222): Show |
1 | a0001c0001t0001g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2106+119_2106+120i others(231): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459951 | ||||||
chr13:48459951 | T | TTTC | 20 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0026 others(17): Show |
20 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.2106+120_2106+121i others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459951 | ||||||
chr13:48459951 | TTTTCTTT others(21): Show |
T | 10 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0239 others(7): Show |
10 | HG02572.hp2 HG02647.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2106+122_2106+149d others(30): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459951 | ||||||
chr13:48459952 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2106+119T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459952 | |||||||
chr13:48459953 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2106+120T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459953 | |||||||
chr13:48459954 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
41 | HG00558.hp2 HG00609.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.2106+121T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459954 | |||||||
chr13:48459955 | C | CT | 19 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0026 others(16): Show |
19 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.2106+125dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459955 | ||||||
chr13:48459955 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
41 | HG00558.hp2 HG00609.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.2106+122C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459955 | |||||||
chr13:48459956 | T | TTCTCTTC others(137): Show |
1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2106+124_2106+125i others(146): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459956 | ||||||
chr13:48459959 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(106): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2106+129dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459959 | ||||||
chr13:48459959 | CT | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(21): Show |
25 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(22): Show |
intron_variant | MODIFIER | c.2106+129delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459959 | ||||||
chr13:48459963 | C | T | 8 | a0001c0001t0001g0235 a0001c0001t0001g0275 a0001c0001t0001g0278 others(5): Show |
8 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2106+130C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459963 | |||||||
chr13:48459964 | T | C | 8 | a0001c0001t0001g0235 a0001c0001t0001g0275 a0001c0001t0001g0278 others(5): Show |
8 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2106+131T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459964 | |||||||
chr13:48459965 | TTCTCTCT others(7): Show |
T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0236 a0001c0001t0001g0242 others(1): Show |
4 | HG01496.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+134_2106+147d others(16): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459965 | ||||||
chr13:48459967 | C | T | 8 | a0001c0001t0001g0235 a0001c0001t0001g0275 a0001c0001t0001g0278 others(5): Show |
8 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2106+134C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459967 | |||||||
chr13:48459967 | CTCTCTTT others(3): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2106+138_2106+147d others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459967 | ||||||
chr13:48459968 | TC | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2106+136delC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459968 | |||||||
chr13:48459968 | TCTC | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+136_2106+138d others(5): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459968 | |||||||
chr13:48459969 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.2106+136C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459969 | |||||||
chr13:48459970 | TC | T | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2106+138delC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459970 | |||||||
chr13:48459971 | C | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+138C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459971 | |||||||
chr13:48459972 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(27): Show |
31 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.2106+139T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459972 | |||||||
chr13:48459973 | TTC | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(28): Show |
32 | HG00741.hp2 HG01074.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.2106+142_2106+143d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459973 | ||||||
chr13:48459974 | T | C | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+141T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459974 | |||||||
chr13:48459975 | C | CCT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
56 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.2106+142_2106+143i others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459975 | |||||||
chr13:48459975 | C | CTT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0280 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2106+144_2106+145d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459975 | ||||||
chr13:48459975 | C | CTTTTCTT others(16): Show |
1 | a0001c0001t0001g0180 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2106+145_2106+146i others(25): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459975 | ||||||
chr13:48459975 | C | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(7): Show |
10 | HG00558.hp2 HG01109.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.2106+142C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459975 | |||||||
chr13:48459977 | TTC | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0200 a0001c0001t0001g0240 others(25): Show |
29 | HG00323.hp2 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.2106+146_2106+147d others(4): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459977 | ||||||
chr13:48459979 | C | CCTTTTT | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2106+146_2106+147i others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459979 | |||||||
chr13:48459979 | C | CTTTTCTT others(20): Show |
1 | a0001c0001t0001g0021 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2106+150_2106+151i others(29): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459979 | ||||||
chr13:48459979 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
102 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.2106+146C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459979 | |||||||
chr13:48459981 | T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2106+149_2106+150i others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr13 | 48459981 | ||||||
chr13:48459983 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2106+150T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459983 | |||||||
chr13:48459983 | T | TC | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+150_2106+151i others(3): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459983 | |||||||
chr13:48459984 | T | C | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2106+151T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459984 | |||||||
chr13:48459987 | TGAGATAG | T | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2106+155_2106+161d others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459987 | |||||||
chr13:48459988 | G | C | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+155G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459988 | |||||||
chr13:48459989 | A | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+156A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459989 | |||||||
chr13:48459990 | G | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+157G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459990 | |||||||
chr13:48459991 | A | C | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+158A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459991 | |||||||
chr13:48459993 | A | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+160A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459993 | |||||||
chr13:48459994 | G | T | 6 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(3): Show |
6 | HG00558.hp2 HG01109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+161G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459994 | |||||||
chr13:48459995 | A | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2106+162A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459995 | |||||||
chr13:48459996 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2106+163G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48459996 | |||||||
chr13:48460018 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2106+185A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460018 | |||||||
chr13:48460040 | G | T | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2106+207G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460040 | |||||||
chr13:48460169 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | NA19060.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2106+336A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460169 | |||||||
chr13:48460256 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2106+423C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460256 | |||||||
chr13:48460268 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2106+435C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460268 | |||||||
chr13:48460295 | A | G | 6 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0190 others(3): Show |
6 | HG02257.hp2 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2106+462A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460295 | |||||||
chr13:48460420 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+587G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460420 | |||||||
chr13:48460488 | C | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(263): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.2106+655C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460488 | |||||||
chr13:48460541 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2106+708A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460541 | |||||||
chr13:48460600 | A | G | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2106+767A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460600 | |||||||
chr13:48460645 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+812C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460645 | |||||||
chr13:48460899 | T | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0080 |
3 | HG03491.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2106+1066T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48460899 | |||||||
chr13:48461035 | A | T | 1 | a0001c0001t0001g0247 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2106+1202A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461035 | |||||||
chr13:48461090 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2106+1257T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461090 | |||||||
chr13:48461104 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2106+1271T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461104 | |||||||
chr13:48461157 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0047 |
2 | HG00558.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2106+1324A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461157 | |||||||
chr13:48461277 | G | A | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+1444G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461277 | |||||||
chr13:48461331 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(88): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.2106+1498T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461331 | |||||||
chr13:48461459 | A | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2106+1626A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461459 | |||||||
chr13:48461557 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2106+1724G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461557 | |||||||
chr13:48461717 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2106+1884G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461717 | |||||||
chr13:48461805 | T | C | 7 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107-1926T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461805 | |||||||
chr13:48461871 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2107-1860C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461871 | |||||||
chr13:48461895 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2107-1836C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461895 | |||||||
chr13:48461943 | C | T | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107-1788C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48461943 | |||||||
chr13:48462106 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2107-1625C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462106 | |||||||
chr13:48462179 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2107-1552A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462179 | |||||||
chr13:48462411 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
7 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107-1320C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462411 | |||||||
chr13:48462493 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2107-1238A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462493 | |||||||
chr13:48462513 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107-1218A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462513 | |||||||
chr13:48462718 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2107-1013A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462718 | |||||||
chr13:48462837 | T | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2107-894T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462837 | |||||||
chr13:48462897 | T | G | 4 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG00738.hp1 HG02055.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107-834T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48462897 | |||||||
chr13:48463301 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2107-430C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 20/26 | chr13 | 48463301 | |||||||
chr13:48464323 | A | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2211+488A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464323 | |||||||
chr13:48464541 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2212-457G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464541 | |||||||
chr13:48464567 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2212-431T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464567 | |||||||
chr13:48464619 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG00609.hp1 NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2212-379G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464619 | |||||||
chr13:48464696 | C | T | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-302C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464696 | |||||||
chr13:48464853 | T | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2212-145T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464853 | |||||||
chr13:48464958 | C | CT | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(90): Show |
93 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2212-16dupT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 48464958 | ||||||
chr13:48464958 | C | CTT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0016 others(5): Show |
8 | HG00741.hp2 HG02056.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2212-17_2212-16dup others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 48464958 | ||||||
chr13:48464958 | CT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2212-16delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 48464958 | ||||||
chr13:48464958 | CTT | C | 19 | a0001c0001t0001g0197 a0001c0001t0001g0201 a0001c0001t0001g0202 others(16): Show |
20 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.2212-17_2212-16del others(2): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | INFO_REALIGN_3_PRIME | chr13 | 48464958 | ||||||
chr13:48464982 | T | A | 7 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2212-16T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 21/26 | chr13 | 48464982 | |||||||
chr13:48465471 | T | A | 1 | a0001c0001t0005g0290 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2489+103T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465471 | |||||||
chr13:48465582 | G | T | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2489+214G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465582 | |||||||
chr13:48465617 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.2489+249G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465617 | |||||||
chr13:48465617 | G | T | 5 | a0001c0001t0001g0289 a0001c0001t0005g0290 a0001c0001t0005g0291 others(2): Show |
5 | HG01975.hp1 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489+249G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465617 | |||||||
chr13:48465675 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0183 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2489+307C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465675 | |||||||
chr13:48465688 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2489+320C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465688 | |||||||
chr13:48465694 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2489+326T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465694 | |||||||
chr13:48465711 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2489+343C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465711 | |||||||
chr13:48465712 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2489+344G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465712 | |||||||
chr13:48465861 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+493A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465861 | |||||||
chr13:48465865 | C | T | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489+497C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465865 | |||||||
chr13:48465910 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+542C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465910 | |||||||
chr13:48465922 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2489+554C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465922 | |||||||
chr13:48465969 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2489+601C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465969 | |||||||
chr13:48465976 | G | C | 3 | a0001c0001t0001g0209 a0003c0003t0001g0210 a0003c0003t0001g0211 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2489+608G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465976 | |||||||
chr13:48465990 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2489+622T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48465990 | |||||||
chr13:48466027 | C | T | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+659C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466027 | |||||||
chr13:48466253 | G | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2489+885G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466253 | |||||||
chr13:48466259 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489+891C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466259 | |||||||
chr13:48466291 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2489+923G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466291 | |||||||
chr13:48466312 | A | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2489+944A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466312 | |||||||
chr13:48466312 | A | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2489+944A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466312 | |||||||
chr13:48466316 | A | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2489+948A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466316 | |||||||
chr13:48466322 | T | C | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2489+954T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466322 | |||||||
chr13:48466394 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
87 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.2489+1026G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466394 | |||||||
chr13:48466616 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2489+1248C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466616 | |||||||
chr13:48466628 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2489+1260C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466628 | |||||||
chr13:48466738 | G | C | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489+1370G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466738 | |||||||
chr13:48466738 | G | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2489+1370G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466738 | |||||||
chr13:48466743 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2489+1375G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466743 | |||||||
chr13:48466779 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0245 |
2 | NA18987.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2489+1411A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466779 | |||||||
chr13:48466784 | G | A | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489+1416G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466784 | |||||||
chr13:48466838 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2489+1470T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466838 | |||||||
chr13:48466889 | C | T | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2489+1521C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466889 | |||||||
chr13:48466951 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2489+1583T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466951 | |||||||
chr13:48466952 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2489+1584G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466952 | |||||||
chr13:48466953 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2489+1585T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48466953 | |||||||
chr13:48467033 | G | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2489+1665G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467033 | |||||||
chr13:48467038 | G | A | 14 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0205 others(11): Show |
14 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2489+1670G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467038 | |||||||
chr13:48467058 | C | T | 6 | a0001c0001t0001g0135 a0001c0001t0001g0156 a0001c0001t0001g0160 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.2489+1690C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467058 | |||||||
chr13:48467116 | C | T | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2489+1748C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467116 | |||||||
chr13:48467140 | G | A | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2489+1772G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467140 | |||||||
chr13:48467397 | T | G | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0273 |
3 | NA18979.hp1 NA18987.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2489+2029T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467397 | |||||||
chr13:48467410 | G | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0100 others(13): Show |
16 | HG00609.hp1 HG01255.hp1 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.2489+2042G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467410 | |||||||
chr13:48467433 | G | A | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489+2065G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467433 | |||||||
chr13:48467442 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2489+2074C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467442 | |||||||
chr13:48467504 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2489+2136T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467504 | |||||||
chr13:48467528 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+2160A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467528 | |||||||
chr13:48467611 | G | A | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2489+2243G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467611 | |||||||
chr13:48467728 | T | C | 4 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0243 others(1): Show |
4 | HG01109.hp2 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2489+2360T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467728 | |||||||
chr13:48467767 | G | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2489+2399G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467767 | |||||||
chr13:48467791 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489+2423A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467791 | |||||||
chr13:48467794 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.2489+2426G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467794 | |||||||
chr13:48467870 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
260 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.2489+2502G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467870 | |||||||
chr13:48467917 | G | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489+2549G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48467917 | |||||||
chr13:48468027 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2489+2659A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468027 | |||||||
chr13:48468055 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2489+2687A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468055 | |||||||
chr13:48468088 | C | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+2720C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468088 | |||||||
chr13:48468097 | A | G | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0212 others(17): Show |
20 | HG00738.hp2 HG01168.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2489+2729A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468097 | |||||||
chr13:48468102 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2489+2734A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468102 | |||||||
chr13:48468106 | C | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0071 others(16): Show |
19 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2489+2738C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468106 | |||||||
chr13:48468226 | A | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489+2858A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468226 | |||||||
chr13:48468284 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2489+2916C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468284 | |||||||
chr13:48468356 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2489+2988A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468356 | |||||||
chr13:48468397 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2489+3029C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468397 | |||||||
chr13:48468488 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2489+3120C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468488 | |||||||
chr13:48468563 | G | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+3195G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468563 | |||||||
chr13:48468598 | TC | T | 8 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489+3231delC | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468598 | |||||||
chr13:48468599 | CA | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(243): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.2489+3238delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48468599 | ||||||
chr13:48468600 | A | T | 8 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(5): Show |
8 | HG01109.hp2 HG02630.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2489+3232A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468600 | |||||||
chr13:48468658 | C | T | 2 | a0002c0002t0001g0250 a0002c0002t0001g0253 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2489+3290C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468658 | |||||||
chr13:48468659 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0118 |
2 | HG04228.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.2489+3291G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468659 | |||||||
chr13:48468724 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2489+3356G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468724 | |||||||
chr13:48468819 | G | T | 13 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(10): Show |
14 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.2489+3451G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468819 | |||||||
chr13:48468823 | C | A | 3 | a0001c0001t0001g0285 a0001c0001t0005g0292 a0001c0001t0005g0293 |
3 | HG00323.hp2 HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2489+3455C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468823 | |||||||
chr13:48468830 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2489+3462C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468830 | |||||||
chr13:48468831 | G | A | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2489+3463G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468831 | |||||||
chr13:48468940 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2489+3572G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468940 | |||||||
chr13:48468965 | C | T | 1 | a0001c0001t0008g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2489+3597C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48468965 | |||||||
chr13:48469048 | C | G | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2489+3680C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469048 | |||||||
chr13:48469064 | G | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+3696G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469064 | |||||||
chr13:48469104 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2489+3736G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469104 | |||||||
chr13:48469180 | G | A | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2489+3812G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469180 | |||||||
chr13:48469260 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2489+3892C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469260 | |||||||
chr13:48469354 | T | C | 1 | a0004c0006t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2489+3986T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469354 | |||||||
chr13:48469451 | T | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490-3909T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469451 | |||||||
chr13:48469526 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0003g0004 a0001c0001t0003g0120 others(1): Show |
5 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2490-3834G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469526 | |||||||
chr13:48469538 | C | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2490-3822C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469538 | |||||||
chr13:48469562 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2490-3798G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469562 | |||||||
chr13:48469598 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2490-3762A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469598 | |||||||
chr13:48469667 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2490-3693C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469667 | |||||||
chr13:48469670 | C | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2490-3690C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469670 | |||||||
chr13:48469678 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2490-3682A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469678 | |||||||
chr13:48469699 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.2490-3661G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469699 | |||||||
chr13:48469851 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2490-3509A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48469851 | |||||||
chr13:48470007 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2490-3353G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470007 | |||||||
chr13:48470075 | A | G | 23 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(20): Show |
23 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2490-3285A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470075 | |||||||
chr13:48470083 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0120 a0001c0001t0003g0121 |
4 | HG01192.hp2 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490-3277A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470083 | |||||||
chr13:48470089 | G | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490-3271G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470089 | |||||||
chr13:48470095 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2490-3265G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470095 | |||||||
chr13:48470256 | C | A | 1 | a0001c0001t0001g0272 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2490-3104C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470256 | |||||||
chr13:48470494 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2490-2866T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470494 | |||||||
chr13:48470496 | G | C | 1 | a0001c0001t0001g0037 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2490-2864G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470496 | |||||||
chr13:48470499 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2490-2861G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470499 | |||||||
chr13:48470579 | C | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0213 a0001c0001t0001g0220 |
3 | HG01884.hp1 HG02886.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2490-2781C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470579 | |||||||
chr13:48470591 | C | T | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2490-2769C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470591 | |||||||
chr13:48470592 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0213 a0001c0001t0001g0220 |
3 | HG01884.hp1 HG02886.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2490-2768G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470592 | |||||||
chr13:48470652 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2490-2708G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470652 | |||||||
chr13:48470659 | A | ACT | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2490-2699_2490-269 others(6): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48470659 | ||||||
chr13:48470678 | A | G | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490-2682A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470678 | |||||||
chr13:48470683 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2490-2677C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470683 | |||||||
chr13:48470721 | A | AAAAC | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2490-2636_2490-263 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48470721 | ||||||
chr13:48470731 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2490-2629T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470731 | |||||||
chr13:48470854 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2490-2506T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470854 | |||||||
chr13:48470863 | T | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2490-2497T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470863 | |||||||
chr13:48470936 | A | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0234 a0001c0001t0001g0235 others(35): Show |
40 | HG00323.hp2 HG00558.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.2490-2424A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48470936 | |||||||
chr13:48471169 | A | C | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2490-2191A>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471169 | |||||||
chr13:48471352 | T | C | 25 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0260 others(22): Show |
26 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.2490-2008T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471352 | |||||||
chr13:48471407 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.2490-1953T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471407 | |||||||
chr13:48471468 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2490-1892C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471468 | |||||||
chr13:48471567 | T | TA | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490-1792dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48471567 | ||||||
chr13:48471569 | T | A | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2490-1791T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471569 | |||||||
chr13:48471573 | T | TAAAA | 10 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
10 | HG01496.hp2 HG02145.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2490-1776_2490-177 others(8): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48471573 | ||||||
chr13:48471573 | T | TAAAAA | 22 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0204 others(19): Show |
22 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2490-1777_2490-177 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48471573 | ||||||
chr13:48471573 | T | TAAAAAA | 5 | a0001c0001t0001g0248 a0001c0001t0001g0273 a0001c0001t0003g0004 others(2): Show |
6 | HG01192.hp2 HG01884.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490-1778_2490-177 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48471573 | ||||||
chr13:48471573 | T | TAAAAAAA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0259 a0001c0001t0001g0261 others(20): Show |
24 | HG00323.hp2 HG02129.hp1 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.2490-1779_2490-177 others(11): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr13 | 48471573 | ||||||
chr13:48471573 | T | TTAAAA | 5 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0071 others(2): Show |
5 | HG01258.hp2 HG01496.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.2490-1787_2490-178 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471573 | |||||||
chr13:48471573 | T | TTAAAAA | 105 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(102): Show |
105 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.2490-1787_2490-178 others(10): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471573 | |||||||
chr13:48471573 | T | TTAAAAAA | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(67): Show |
75 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.2490-1787_2490-178 others(11): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471573 | |||||||
chr13:48471573 | T | TTAAAAAA others(1): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
9 | HG00408.hp1 HG00609.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2490-1787_2490-178 others(12): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471573 | |||||||
chr13:48471573 | T | TTAAAAAA others(2): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | NA18906.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2490-1787_2490-178 others(13): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471573 | |||||||
chr13:48471577 | A | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490-1783A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471577 | |||||||
chr13:48471583 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2490-1777A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471583 | |||||||
chr13:48471654 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2490-1706C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48471654 | |||||||
chr13:48472031 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2490-1329C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48472031 | |||||||
chr13:48472037 | C | T | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2490-1323C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48472037 | |||||||
chr13:48472103 | T | C | 1 | a0001c0007t0001g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2490-1257T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48472103 | |||||||
chr13:48472191 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0280 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2490-1169G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48472191 | |||||||
chr13:48472721 | A | G | 2 | a0002c0002t0001g0251 a0002c0002t0001g0252 |
2 | HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2490-639A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48472721 | |||||||
chr13:48473176 | G | C | 1 | a0001c0001t0001g0234 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2490-184G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48473176 | |||||||
chr13:48473266 | T | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2490-94T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48473266 | |||||||
chr13:48473281 | A | G | 7 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2490-79A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48473281 | |||||||
chr13:48473315 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2490-45A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 23/26 | chr13 | 48473315 | |||||||
chr13:48473795 | G | A | 21 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(18): Show |
21 | HG00609.hp1 HG01071.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2520+405G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48473795 | |||||||
chr13:48473908 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2520+518C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48473908 | |||||||
chr13:48474037 | G | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0275 others(7): Show |
10 | HG00558.hp2 HG01109.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.2520+647G>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474037 | |||||||
chr13:48474180 | G | T | 2 | a0001c0001t0002g0198 a0001c0001t0002g0199 |
2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2520+790G>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474180 | |||||||
chr13:48474203 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2520+813T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474203 | |||||||
chr13:48474288 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2520+898A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474288 | |||||||
chr13:48474474 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0019 |
2 | HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2520+1084A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474474 | |||||||
chr13:48474492 | C | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
264 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.2520+1102C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474492 | |||||||
chr13:48474621 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
227 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.2520+1231C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474621 | |||||||
chr13:48474783 | T | C | 6 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0105 others(3): Show |
6 | HG01255.hp1 HG02004.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.2520+1393T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474783 | |||||||
chr13:48474807 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2520+1417T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474807 | |||||||
chr13:48474893 | T | C | 4 | a0001c0001t0005g0290 a0001c0001t0005g0291 a0001c0001t0005g0292 others(1): Show |
4 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2520+1503T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474893 | |||||||
chr13:48474923 | C | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2520+1533C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48474923 | |||||||
chr13:48475072 | T | C | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0247 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2521-1629T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475072 | |||||||
chr13:48475096 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
237 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.2521-1605C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475096 | |||||||
chr13:48475109 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2521-1592C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475109 | |||||||
chr13:48475110 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2521-1591G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475110 | |||||||
chr13:48475203 | C | G | 1 | a0002c0002t0001g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2521-1498C>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475203 | |||||||
chr13:48475353 | TTGGGC | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2521-1342_2521-133 others(9): Show |
RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr13 | 48475353 | ||||||
chr13:48475457 | A | G | 3 | a0001c0001t0004g0237 a0001c0001t0004g0238 a0001c0001t0004g0246 |
3 | HG02630.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2521-1244A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475457 | |||||||
chr13:48475531 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0079 |
2 | NA19004.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2521-1170C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475531 | |||||||
chr13:48475953 | A | G | 2 | a0001c0001t0001g0203 a0001c0007t0001g0207 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2521-748A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48475953 | |||||||
chr13:48476026 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2521-675C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48476026 | |||||||
chr13:48476112 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2521-589G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48476112 | |||||||
chr13:48476690 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2521-11G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 24/26 | chr13 | 48476690 | |||||||
chr13:48476876 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2663+33C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 25/26 | chr13 | 48476876 | |||||||
chr13:48476913 | G | A | 1 | a0005c0005t0001g0294 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2663+70G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 25/26 | chr13 | 48476913 | |||||||
chr13:48477173 | A | G | 1 | a0004c0006t0001g0173 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2664-182A>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 25/26 | chr13 | 48477173 | |||||||
chr13:48477345 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(66): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2664-10T>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 25/26 | chr13 | 48477345 | |||||||
chr13:48477570 | A | T | 7 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
7 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2713+166A>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48477570 | |||||||
chr13:48477712 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(261): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2713+308G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48477712 | |||||||
chr13:48477997 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2713+593G>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48477997 | |||||||
chr13:48477998 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2713+594T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48477998 | |||||||
chr13:48478233 | C | A | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(1): Show |
4 | HG03453.hp1 NA19030.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2713+829C>A | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48478233 | |||||||
chr13:48478754 | T | G | 19 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0201 others(16): Show |
19 | HG01243.hp2 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2714-1244T>G | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48478754 | |||||||
chr13:48478769 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2714-1229C>T | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48478769 | |||||||
chr13:48479227 | C | CA | 8 | a0001c0001t0001g0081 a0001c0001t0001g0221 a0001c0001t0001g0224 others(5): Show |
8 | HG02257.hp1 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2714-759dupA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr13 | 48479227 | ||||||
chr13:48479227 | CA | C | 7 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0190 others(4): Show |
7 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2714-759delA | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr13 | 48479227 | ||||||
chr13:48479244 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2714-754T>C | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | chr13 | 48479244 | |||||||
chr13:48479655 | AT | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0109 a0001c0001t0001g0110 others(6): Show |
9 | HG00609.hp1 HG02257.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2714-333delT | RB1 | ENSG00000139687.16 | transcript | ENST00000267163.6 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr13 | 48479655 |