Item | Value |
---|---|
geneid | 55920 |
ensemblid | ENSG00000179051.14 |
hgncid | 30297 |
symbol | RCC2 |
name | regulator of chromosome condensation 2 |
refseq_nuc | NM_018715.4 |
refseq_prot | NP_061185.1 |
ensembl_nuc | ENST00000375436.9 |
ensembl_prot | ENSP00000364585.4 |
mane_status | MANE Select |
chr | chr1 |
start | 17406760 |
end | 17439677 |
strand | - |
ver | v1.2 |
region | chr1:17406760-17439677 |
region5000 | chr1:17401760-17444677 |
regionname0 | RCC2_chr1_17406760_17439677 |
regionname5000 | RCC2_chr1_17401760_17444677 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 522 | 376 | 86 | 73 | 158 | 12 | 45 | 124 | RCC2_chr1_17401760_17444677 | RCC2 | MPRKK others(517): Show |
chr1 | 17401760 | 17444677 |
a0002 | 0/0 | 522 | 11 | 8 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | MPRKK others(517): Show |
chr1 | 17401760 | 17444677 |
a0003 | 0/0 | 522 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | MPRKK others(517): Show |
chr1 | 17401760 | 17444677 |
a0004 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | MPRKK others(517): Show |
chr1 | 17401760 | 17444677 |
a0005 | 0/0 | 522 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | MPRKK others(517): Show |
chr1 | 17401760 | 17444677 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1566 | 261 | 52 | 40 | 131 | 8 | 28 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0002 | 0/0 | 1566 | 108 | 31 | 32 | 25 | 4 | 16 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0004 | 0/0 | 1566 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0007 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0009 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0011 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0001c0012 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0002c0003 | 0/0 | 1566 | 10 | 7 | 3 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0002c0005 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0003c0006 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0004c0008 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 | ||
a0005c0010 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | ATGCC others(1561): Show |
chr1 | 17401760 | 17444677 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4040 | 125 | 25 | 22 | 59 | 4 | 13 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0003 | 0/0 | 4037 | 54 | 2 | 0 | 48 | 1 | 3 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0004 | 0/0 | 4037 | 40 | 6 | 11 | 13 | 2 | 8 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0006 | 0/0 | 4038 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4033): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0007 | 0/0 | 4034 | 7 | 2 | 1 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4029): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0008 | 0/0 | 4037 | 6 | 6 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0009 | 0/0 | 4041 | 5 | 3 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4036): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0010 | 0/0 | 4036 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4031): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0014 | 0/0 | 4037 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0016 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0017 | 0/0 | 4036 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4031): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0018 | 0/0 | 4039 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4034): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0019 | 0/0 | 4039 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4034): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0021 | 0/0 | 4030 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4025): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0022 | 0/0 | 4040 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0023 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0024 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0025 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0026 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0027 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0028 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0029 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0030 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0031 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0034 | 0/0 | 4037 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0001t0035 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0002 | 0/0 | 4037 | 82 | 25 | 21 | 23 | 3 | 10 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0004 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0005 | 0/0 | 4037 | 15 | 3 | 7 | 0 | 0 | 5 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0011 | 0/0 | 4037 | 3 | 0 | 2 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0012 | 0/0 | 4036 | 2 | 1 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4031): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0013 | 0/0 | 4036 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4031): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0020 | 0/0 | 4036 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4031): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0032 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0002t0033 | 0/0 | 4037 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0004t0004 | 0/0 | 4037 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0001c0007t0001 | 0/0 | 4040 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0009t0001 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0011t0001 | 0/0 | 4040 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4035): Show |
chr1 | 17401760 | 17444677 |
a0001c0012t0002 | 0/0 | 4037 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0002c0003t0004 | 0/0 | 4037 | 3 | 3 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0002c0003t0006 | 0/0 | 4038 | 5 | 3 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4033): Show |
chr1 | 17401760 | 17444677 |
a0002c0003t0015 | 0/0 | 4038 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4033): Show |
chr1 | 17401760 | 17444677 |
a0002c0005t0006 | 0/0 | 4038 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4033): Show |
chr1 | 17401760 | 17444677 |
a0003c0006t0003 | 0/0 | 4037 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0004c0008t0002 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
a0005c0010t0003 | 0/0 | 4037 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | GTATT others(4032): Show |
chr1 | 17401760 | 17444677 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0013 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0006g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0010g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0014g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0016g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0017g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0018g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0019g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0021g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0022g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0023g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0024g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0025g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0026g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0027g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0028g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0029g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0030g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0031g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0034g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0001t0035g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0010 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0011g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0012g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0013g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0020g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0032g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0002t0033g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0004t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0004t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0009t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0011t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0001c0012t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0015g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0003t0015g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0002c0005t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0003c0006t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0004c0008t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
a0005c0010t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0232 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00140 | hp2 | a0001 | c0002 | t0011 | g0185 | EUR | GBR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00280 | hp1 | a0001 | c0001 | t0024 | g0070 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0022 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0266 | EUR | FIN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00639 | hp1 | a0001 | c0001 | t0034 | g0207 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0233 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00642 | hp1 | a0001 | c0002 | t0020 | g0299 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00738 | hp1 | a0001 | c0002 | t0005 | g0173 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0030 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01070 | hp2 | a0001 | c0002 | t0013 | g0051 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01071 | hp1 | a0001 | c0002 | t0005 | g0050 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01071 | hp2 | a0001 | c0001 | t0009 | g0238 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0306 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01081 | hp2 | a0001 | c0002 | t0005 | g0147 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01099 | hp1 | a0002 | c0003 | t0006 | g0289 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01106 | hp1 | a0002 | c0003 | t0006 | g0290 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0308 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01168 | hp2 | a0001 | c0002 | t0011 | g0202 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01169 | hp2 | a0001 | c0002 | t0011 | g0201 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0177 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01243 | hp2 | a0002 | c0003 | t0015 | g0288 | AMR | PUR | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0144 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0198 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0145 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01361 | hp2 | a0001 | c0012 | t0002 | g0279 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01433 | hp2 | a0001 | c0002 | t0005 | g0021 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0274 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0191 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0194 | EUR | IBS | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01884 | hp2 | a0002 | c0003 | t0006 | g0032 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01891 | hp2 | a0002 | c0003 | t0004 | g0284 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01928 | hp2 | a0001 | c0001 | t0021 | g0129 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01943 | hp1 | a0001 | c0001 | t0019 | g0098 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0209 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0026 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0211 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02004 | hp2 | a0001 | c0002 | t0005 | g0165 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02040 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0304 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02145 | hp2 | a0002 | c0003 | t0015 | g0285 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0303 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0172 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0157 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0313 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | PEL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0296 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0314 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0030 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02622 | hp1 | a0002 | c0003 | t0006 | g0032 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0305 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0311 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02683 | hp2 | a0003 | c0006 | t0003 | g0205 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0269 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0302 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02735 | hp1 | a0001 | c0002 | t0005 | g0021 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02738 | hp1 | a0001 | c0002 | t0032 | g0175 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0010 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02809 | hp1 | a0001 | c0004 | t0004 | g0035 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02818 | hp2 | a0002 | c0003 | t0004 | g0286 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02886 | hp2 | a0001 | c0001 | t0029 | g0236 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02895 | hp2 | a0001 | c0001 | t0028 | g0252 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0312 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02965 | hp1 | a0001 | c0002 | t0013 | g0168 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02965 | hp2 | a0002 | c0003 | t0004 | g0283 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0166 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02976 | hp1 | a0001 | c0002 | t0033 | g0300 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02976 | hp2 | a0001 | c0001 | t0022 | g0106 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03017 | hp1 | a0001 | c0001 | t0035 | g0326 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03017 | hp2 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03098 | hp1 | a0002 | c0005 | t0006 | g0291 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03130 | hp2 | a0001 | c0002 | t0005 | g0170 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0161 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03209 | hp1 | a0001 | c0004 | t0004 | g0035 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0189 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0156 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03516 | hp2 | a0001 | c0002 | t0012 | g0325 | AFR | ESN | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0200 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0143 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0248 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03710 | hp1 | a0001 | c0002 | t0005 | g0149 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0162 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03942 | hp1 | a0001 | c0001 | t0014 | g0247 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04115 | hp1 | a0001 | c0002 | t0005 | g0320 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0036 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0010 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04184 | hp2 | a0001 | c0007 | t0001 | g0059 | SAS | BEB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0256 | SAS | STU | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18747 | hp1 | a0001 | c0002 | t0012 | g0184 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | CHB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0298 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18946 | hp1 | a0001 | c0001 | t0026 | g0206 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18946 | hp2 | a0001 | c0001 | t0023 | g0099 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18963 | hp2 | a0001 | c0001 | t0007 | g0275 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18964 | hp1 | a0001 | c0001 | t0030 | g0108 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0277 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA18994 | hp2 | a0001 | c0011 | t0001 | g0142 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19030 | hp1 | a0001 | c0001 | t0027 | g0292 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0297 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19055 | hp2 | a0001 | c0001 | t0010 | g0223 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19058 | hp1 | a0004 | c0008 | t0002 | g0182 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19079 | hp1 | a0005 | c0010 | t0003 | g0323 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19081 | hp1 | a0001 | c0009 | t0001 | g0076 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19084 | hp1 | a0001 | c0001 | t0025 | g0265 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19087 | hp2 | a0001 | c0001 | t0007 | g0276 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19089 | hp1 | a0001 | c0001 | t0010 | g0224 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19089 | hp2 | a0001 | c0001 | t0018 | g0084 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | YRI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ASW | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | ASW | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0013 | EUR | TSI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0159 | EUR | TSI | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20905 | hp2 | a0001 | c0001 | t0014 | g0249 | SAS | GIH | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0193 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02109 | hp2 | a0001 | c0002 | t0005 | g0049 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02486 | hp2 | a0002 | c0003 | t0006 | g0287 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0295 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03471 | hp1 | a0001 | c0001 | t0031 | g0037 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | MSL | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0315 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0278 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | USA | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0301 | AFR | LWK | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0063 | REF | REF | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0091 | REF | REF | RCC2_chr1_17401760_17444677 | RCC2 | chr1 | 17401760 | 17444677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17420785 | G | C | 1 | a0004 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.788C>G | p.Ala263Gly | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/13 | 929/4040 | 788/1569 | 263/522 | chr1 | 17420785 | |||
chr1:17420786 | C | G | 1 | a0004 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.787G>C | p.Ala263Pro | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/13 | 928/4040 | 787/1569 | 263/522 | chr1 | 17420786 | |||
chr1:17422289 | T | C | 1 | a0005 | 1 | NA19079.hp1 | missense_variant&splice_region_variant | MODERATE | c.658A>G | p.Thr220Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/13 | 799/4040 | 658/1569 | 220/522 | chr1 | 17422289 | |||
chr1:17438267 | A | G | 1 | a0003 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.248T>C | p.Val83Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 389/4040 | 248/1569 | 83/522 | chr1 | 17438267 | |||
chr1:17438292 | C | T | 1 | a0002 | 11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
missense_variant | MODERATE | c.223G>A | p.Ala75Thr | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 364/4040 | 223/1569 | 75/522 | chr1 | 17438292 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17413090 | G | A | 4 | a0001c0002 a0001c0012 a0002c0005 others(1): Show |
111 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(108): Show |
synonymous_variant | LOW | c.1296C>T | p.Ile432Ile | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/13 | 1437/4040 | 1296/1569 | 432/522 | chr1 | 17413090 | |||
chr1:17413550 | A | G | 1 | a0001c0009 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.1194T>C | p.Ala398Ala | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/13 | 1335/4040 | 1194/1569 | 398/522 | chr1 | 17413550 | |||
chr1:17416549 | C | T | 1 | a0001c0004 | 3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.957G>A | p.Thr319Thr | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/13 | 1098/4040 | 957/1569 | 319/522 | chr1 | 17416549 | |||
chr1:17438266 | C | T | 1 | a0001c0007 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.249G>A | p.Val83Val | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 390/4040 | 249/1569 | 83/522 | chr1 | 17438266 | |||
chr1:17438278 | G | A | 1 | a0001c0011 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.237C>T | p.Gly79Gly | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 378/4040 | 237/1569 | 79/522 | chr1 | 17438278 | |||
chr1:17438284 | C | T | 2 | a0002c0003 a0002c0005 |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
synonymous_variant | LOW | c.231G>A | p.Lys77Lys | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 372/4040 | 231/1569 | 77/522 | chr1 | 17438284 | |||
chr1:17438299 | C | A | 1 | a0001c0012 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.216G>T | p.Pro72Pro | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/13 | 357/4040 | 216/1569 | 72/522 | chr1 | 17438299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17406771 | ATGT | A | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(29): Show |
247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*2316_*2318delACA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2316 | chr1 | 17406771 | ||||||
chr1:17406859 | C | A | 1 | a0001c0001t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2231G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2231 | chr1 | 17406859 | ||||||
chr1:17407035 | G | A | 2 | a0001c0002t0005 a0001c0002t0013 |
17 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2055C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2055 | chr1 | 17407035 | ||||||
chr1:17407068 | T | G | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(29): Show |
247 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 2022 | chr1 | 17407068 | ||||||
chr1:17407171 | G | A | 1 | a0001c0001t0023 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1919 | chr1 | 17407171 | ||||||
chr1:17407193 | G | A | 1 | a0001c0001t0025 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1897C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1897 | chr1 | 17407193 | ||||||
chr1:17407322 | T | C | 1 | a0001c0001t0019 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1768A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1768 | chr1 | 17407322 | ||||||
chr1:17407393 | G | A | 1 | a0001c0001t0024 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1697 | chr1 | 17407393 | ||||||
chr1:17407500 | G | A | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0025 others(3): Show |
61 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1590C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1590 | chr1 | 17407500 | ||||||
chr1:17407559 | G | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1531 | chr1 | 17407559 | ||||||
chr1:17407899 | G | A | 1 | a0001c0002t0020 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1191 | chr1 | 17407899 | ||||||
chr1:17407942 | C | A | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1148 | chr1 | 17407942 | ||||||
chr1:17407955 | G | A | 1 | a0001c0001t0028 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1135C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1135 | chr1 | 17407955 | ||||||
chr1:17407974 | C | T | 2 | a0001c0001t0008 a0001c0001t0017 |
7 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1116G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1116 | chr1 | 17407974 | ||||||
chr1:17408047 | T | A | 1 | a0001c0001t0029 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1043A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 1043 | chr1 | 17408047 | ||||||
chr1:17408106 | GAGTCTCA others(3): Show |
G | 1 | a0001c0001t0021 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*974_*983delTGCTGA others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 974 | chr1 | 17408106 | ||||||
chr1:17408131 | G | A | 1 | a0001c0001t0014 | 2 | HG03942.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*959C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 959 | chr1 | 17408131 | ||||||
chr1:17408151 | G | C | 1 | a0001c0002t0011 | 3 | HG00140.hp2 HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 939 | chr1 | 17408151 | ||||||
chr1:17408437 | C | T | 1 | a0001c0001t0007 | 7 | HG01496.hp1 HG03486.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*653G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 653 | chr1 | 17408437 | ||||||
chr1:17408459 | G | C | 1 | a0001c0002t0033 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*631C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 631 | chr1 | 17408459 | ||||||
chr1:17408467 | C | T | 1 | a0002c0003t0015 | 2 | HG01243.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*623G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 623 | chr1 | 17408467 | ||||||
chr1:17408570 | GAGA | G | 1 | a0001c0001t0007 | 7 | HG01496.hp1 HG03486.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*517_*519delTCT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 517 | chr1 | 17408570 | ||||||
chr1:17408585 | G | A | 1 | a0001c0001t0030 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*505C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 505 | chr1 | 17408585 | ||||||
chr1:17408614 | T | G | 1 | a0001c0001t0031 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 476 | chr1 | 17408614 | ||||||
chr1:17408770 | G | A | 10 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0011 others(7): Show |
109 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*320C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 320 | chr1 | 17408770 | ||||||
chr1:17408789 | T | TA | 5 | a0001c0001t0006 a0001c0001t0009 a0002c0003t0006 others(2): Show |
15 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*300dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 300 | chr1 | 17408789 | ||||||
chr1:17408789 | TA | T | 7 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0018 others(4): Show |
11 | HG00639.hp2 HG00642.hp1 HG01070.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*300delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 300 | chr1 | 17408789 | ||||||
chr1:17408844 | T | G | 1 | a0001c0001t0034 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 13/13 | 246 | chr1 | 17408844 | ||||||
chr1:17439582 | A | G | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/13 | 1068 | chr1 | 17439582 | ||||||
chr1:17439634 | G | A | 1 | a0001c0001t0035 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-98C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/13 | chr1 | 17439634 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17409202 | G | T | 6 | a0001c0001t0008g0172 a0001c0001t0008g0311 a0001c0001t0008g0312 others(3): Show |
6 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1465-8C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409202 | |||||||
chr1:17409214 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1465-20A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409214 | |||||||
chr1:17409215 | T | C | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1465-21A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409215 | |||||||
chr1:17409373 | G | A | 4 | a0001c0002t0005g0021 a0001c0002t0005g0165 a0001c0002t0005g0173 others(1): Show |
5 | HG00738.hp1 HG01433.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-179C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409373 | |||||||
chr1:17409423 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1465-229C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409423 | |||||||
chr1:17409424 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1465-230T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409424 | |||||||
chr1:17409464 | G | T | 9 | a0001c0001t0008g0172 a0001c0001t0008g0200 a0001c0001t0008g0311 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1465-270C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409464 | |||||||
chr1:17409504 | C | T | 2 | a0001c0002t0002g0144 a0001c0002t0002g0145 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1465-310G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409504 | |||||||
chr1:17409646 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1464+328C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409646 | |||||||
chr1:17409866 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1464+108C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409866 | |||||||
chr1:17409935 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0066 |
2 | HG02074.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1464+39G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409935 | |||||||
chr1:17409936 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0096 a0001c0001t0001g0100 others(2): Show |
5 | HG00280.hp2 HG01943.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1464+38C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 12/12 | chr1 | 17409936 | |||||||
chr1:17410082 | A | G | 206 | a0001c0001t0001g0072 a0001c0001t0003g0005 a0001c0001t0003g0006 others(203): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1387-31T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410082 | |||||||
chr1:17410409 | G | A | 11 | a0001c0001t0006g0203 a0001c0001t0006g0314 a0002c0003t0004g0283 others(8): Show |
12 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1387-358C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410409 | |||||||
chr1:17410575 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1387-524C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410575 | |||||||
chr1:17410582 | C | T | 1 | a0001c0001t0004g0257 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1387-531G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410582 | |||||||
chr1:17410694 | C | G | 1 | a0002c0003t0004g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1387-643G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410694 | |||||||
chr1:17410890 | G | C | 2 | a0001c0002t0012g0325 a0001c0002t0020g0299 |
2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1387-839C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410890 | |||||||
chr1:17410944 | G | C | 12 | a0001c0002t0002g0004 a0001c0002t0002g0025 a0001c0002t0002g0026 others(9): Show |
18 | HG00741.hp1 HG01081.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1387-893C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17410944 | |||||||
chr1:17411125 | C | A | 1 | a0001c0001t0004g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1386+997G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411125 | |||||||
chr1:17411143 | G | A | 1 | a0002c0003t0004g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1386+979C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411143 | |||||||
chr1:17411315 | G | A | 1 | a0001c0002t0002g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1386+807C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411315 | |||||||
chr1:17411580 | C | CA | 19 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 others(16): Show |
21 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1386+541dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411580 | |||||||
chr1:17411580 | CA | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0067 a0001c0001t0001g0090 others(6): Show |
10 | HG02040.hp2 HG02273.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1386+541delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411580 | |||||||
chr1:17411671 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0017 others(291): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.1386+451A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411671 | |||||||
chr1:17411803 | A | G | 1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1386+319T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411803 | |||||||
chr1:17411826 | CT | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0110 |
3 | NA18977.hp1 NA19010.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1386+295delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17411826 | |||||||
chr1:17412074 | AC | A | 91 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(88): Show |
111 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1386+47delG | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 11/12 | chr1 | 17412074 | |||||||
chr1:17412248 | C | T | 10 | a0001c0001t0006g0203 a0001c0001t0006g0314 a0002c0003t0004g0283 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1314-54G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412248 | |||||||
chr1:17412273 | T | TGTG | 3 | a0002c0003t0006g0289 a0002c0003t0015g0285 a0002c0003t0015g0288 |
3 | HG01099.hp1 HG01243.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1314-82_1314-80dup others(3): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412273 | |||||||
chr1:17412366 | G | C | 1 | a0001c0001t0031g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1314-172C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412366 | |||||||
chr1:17412412 | G | C | 9 | a0001c0001t0008g0172 a0001c0001t0008g0200 a0001c0001t0008g0311 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1314-218C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412412 | |||||||
chr1:17412769 | C | T | 1 | a0001c0001t0004g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1313+304G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412769 | |||||||
chr1:17412817 | T | G | 198 | a0001c0001t0001g0072 a0001c0001t0001g0213 a0001c0001t0003g0005 others(195): Show |
241 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1313+256A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412817 | |||||||
chr1:17412863 | A | G | 1 | a0002c0003t0004g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1313+210T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17412863 | |||||||
chr1:17413021 | C | CA | 8 | a0001c0001t0008g0172 a0001c0001t0008g0200 a0001c0001t0008g0311 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313+51dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413021 | |||||||
chr1:17413023 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0045 others(1): Show |
4 | NA18612.hp1 NA18970.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313+50G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413023 | |||||||
chr1:17413049 | C | T | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1313+24G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 10/12 | chr1 | 17413049 | |||||||
chr1:17413254 | G | C | 1 | a0001c0002t0002g0308 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1208-76C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413254 | |||||||
chr1:17413318 | C | T | 9 | a0001c0001t0008g0172 a0001c0001t0008g0200 a0001c0001t0008g0311 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-140G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413318 | |||||||
chr1:17413324 | T | C | 206 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(203): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.1208-146A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413324 | |||||||
chr1:17413379 | G | C | 1 | a0001c0002t0005g0177 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1207+158C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413379 | |||||||
chr1:17413382 | C | T | 1 | a0001c0001t0003g0239 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1207+155G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413382 | |||||||
chr1:17413523 | C | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0095 others(1): Show |
4 | HG02523.hp2 NA18946.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207+14G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 9/12 | chr1 | 17413523 | |||||||
chr1:17413761 | A | G | 1 | a0001c0001t0029g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1027-44T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413761 | |||||||
chr1:17413838 | A | C | 1 | a0001c0002t0002g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1027-121T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413838 | |||||||
chr1:17413854 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1027-137G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413854 | |||||||
chr1:17413855 | G | A | 1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1027-138C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413855 | |||||||
chr1:17413861 | G | A | 107 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(104): Show |
129 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1027-144C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413861 | |||||||
chr1:17413880 | C | A | 1 | a0001c0001t0004g0246 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-163G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413880 | |||||||
chr1:17413882 | A | C | 1 | a0001c0001t0004g0246 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-165T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413882 | |||||||
chr1:17413883 | C | T | 1 | a0001c0001t0004g0246 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-166G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17413883 | |||||||
chr1:17414007 | A | T | 1 | a0001c0001t0003g0220 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1027-290T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414007 | |||||||
chr1:17414033 | G | A | 2 | a0001c0001t0004g0256 a0001c0001t0029g0236 |
2 | HG02886.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1027-316C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414033 | |||||||
chr1:17414168 | C | A | 1 | a0001c0001t0014g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1027-451G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414168 | |||||||
chr1:17414169 | C | G | 1 | a0001c0002t0002g0192 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1027-452G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414169 | |||||||
chr1:17414183 | G | C | 2 | a0001c0001t0004g0270 a0001c0001t0004g0280 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1027-466C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414183 | |||||||
chr1:17414224 | T | G | 10 | a0001c0001t0006g0203 a0001c0001t0006g0314 a0002c0003t0004g0283 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1027-507A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414224 | |||||||
chr1:17414480 | A | T | 1 | a0002c0005t0006g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1027-763T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414480 | |||||||
chr1:17414529 | C | CA | 6 | a0001c0001t0003g0215 a0001c0001t0003g0222 a0001c0002t0002g0154 others(3): Show |
6 | HG02602.hp1 HG02683.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-813dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414529 | |||||||
chr1:17414529 | CA | C | 8 | a0001c0001t0001g0122 a0001c0001t0008g0172 a0001c0001t0008g0200 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-813delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414529 | |||||||
chr1:17414536 | AAAAAACA others(9): Show |
A | 2 | a0001c0004t0004g0035 a0001c0004t0004g0305 |
3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-835_1027-820d others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414536 | |||||||
chr1:17414537 | A | C | 1 | a0001c0001t0007g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1027-820T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414537 | |||||||
chr1:17414542 | C | A | 1 | a0001c0001t0003g0215 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1027-825G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414542 | |||||||
chr1:17414548 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0061 others(226): Show |
274 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1027-831C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414548 | |||||||
chr1:17414552 | C | CA | 19 | a0001c0001t0003g0241 a0001c0001t0004g0007 a0001c0001t0004g0245 others(16): Show |
19 | HG01081.hp2 HG01175.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1027-836dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414552 | |||||||
chr1:17414559 | A | C | 2 | a0001c0004t0004g0035 a0001c0004t0004g0305 |
3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-842T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414559 | |||||||
chr1:17414566 | C | A | 2 | a0001c0004t0004g0035 a0001c0004t0004g0305 |
3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1027-849G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414566 | |||||||
chr1:17414569 | C | CA | 24 | a0001c0001t0001g0064 a0001c0001t0001g0140 a0001c0001t0001g0281 others(21): Show |
24 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1027-853dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414569 | |||||||
chr1:17414570 | A | C | 1 | a0001c0002t0002g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1027-853T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414570 | |||||||
chr1:17414611 | C | T | 1 | a0001c0002t0002g0304 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1027-894G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414611 | |||||||
chr1:17414631 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1027-914G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414631 | |||||||
chr1:17414646 | C | A | 1 | a0001c0001t0016g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1027-929G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414646 | |||||||
chr1:17414647 | C | T | 1 | a0001c0002t0002g0198 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1027-930G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414647 | |||||||
chr1:17414700 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1027-983G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414700 | |||||||
chr1:17414701 | G | A | 1 | a0001c0002t0011g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1027-984C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414701 | |||||||
chr1:17414745 | C | A | 1 | a0001c0001t0008g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1027-1028G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414745 | |||||||
chr1:17414791 | C | CAGCTGAT others(10): Show |
1 | a0001c0001t0004g0245 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1027-1091_1027-107 others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17414791 | |||||||
chr1:17415035 | G | A | 1 | a0001c0002t0002g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1027-1318C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415035 | |||||||
chr1:17415041 | C | T | 1 | a0001c0001t0004g0246 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1027-1324G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415041 | |||||||
chr1:17415339 | C | G | 10 | a0001c0001t0006g0203 a0001c0001t0006g0314 a0002c0003t0004g0283 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1026+1141G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415339 | |||||||
chr1:17415357 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1026+1123C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415357 | |||||||
chr1:17415495 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1026+985C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415495 | |||||||
chr1:17415528 | T | C | 87 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(84): Show |
107 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1026+952A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415528 | |||||||
chr1:17415713 | T | C | 103 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(100): Show |
124 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1026+767A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415713 | |||||||
chr1:17415714 | A | C | 2 | a0001c0001t0004g0257 a0002c0003t0006g0289 |
2 | HG01099.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1026+766T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415714 | |||||||
chr1:17415717 | A | C | 1 | a0001c0001t0003g0309 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1026+763T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415717 | |||||||
chr1:17415728 | T | C | 2 | a0001c0002t0002g0301 a0001c0002t0002g0302 |
2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1026+752A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415728 | |||||||
chr1:17415838 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1026+642C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415838 | |||||||
chr1:17415839 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026+641A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415839 | |||||||
chr1:17415842 | G | A | 14 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0031 others(11): Show |
19 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1026+638C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415842 | |||||||
chr1:17415845 | G | T | 1 | a0001c0001t0004g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1026+635C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415845 | |||||||
chr1:17415864 | T | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0001g0081 others(5): Show |
9 | HG01891.hp1 HG02257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1026+616A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415864 | |||||||
chr1:17415967 | G | A | 1 | a0001c0001t0004g0250 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1026+513C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415967 | |||||||
chr1:17415999 | G | A | 1 | a0002c0003t0004g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1026+481C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17415999 | |||||||
chr1:17416068 | CA | C | 5 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0005g0021 others(2): Show |
6 | HG01070.hp2 HG01074.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+411delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416068 | |||||||
chr1:17416077 | A | AGG | 4 | a0001c0002t0002g0308 a0002c0003t0006g0287 a0002c0003t0015g0285 others(1): Show |
4 | HG01167.hp2 HG01243.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+402_1026+403i others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416077 | |||||||
chr1:17416078 | A | AG | 87 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
102 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1026+401dupC | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | |||||||
chr1:17416078 | A | AGG | 25 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0044 others(22): Show |
27 | HG00323.hp2 HG00423.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1026+400_1026+401d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | |||||||
chr1:17416078 | A | G | 14 | a0001c0001t0001g0096 a0001c0001t0006g0203 a0001c0001t0006g0314 others(11): Show |
15 | HG00738.hp1 HG01099.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1026+402T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | |||||||
chr1:17416078 | AG | A | 34 | a0001c0001t0003g0012 a0001c0001t0003g0028 a0001c0001t0003g0218 others(31): Show |
41 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1026+401delC | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416078 | |||||||
chr1:17416083 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0111 a0001c0001t0001g0318 |
3 | HG02145.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1026+397C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416083 | |||||||
chr1:17416088 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+392C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416088 | |||||||
chr1:17416089 | G | C | 4 | a0001c0001t0010g0223 a0001c0002t0002g0178 a0001c0002t0002g0180 others(1): Show |
4 | HG02523.hp1 NA19055.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+391C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416089 | |||||||
chr1:17416090 | C | G | 14 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0088 others(11): Show |
14 | HG01167.hp2 HG02280.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1026+390G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416090 | |||||||
chr1:17416117 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1026+363G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416117 | |||||||
chr1:17416118 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1026+362C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416118 | |||||||
chr1:17416429 | C | T | 1 | a0001c0002t0033g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1026+51G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416429 | |||||||
chr1:17416437 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1026+43T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 8/12 | chr1 | 17416437 | |||||||
chr1:17416723 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.860-77A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17416723 | |||||||
chr1:17416859 | C | G | 1 | a0001c0001t0028g0252 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.860-213G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17416859 | |||||||
chr1:17417117 | T | C | 197 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(194): Show |
240 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.860-471A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417117 | |||||||
chr1:17417164 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.860-518C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417164 | |||||||
chr1:17417173 | C | T | 197 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(194): Show |
240 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.860-527G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417173 | |||||||
chr1:17417240 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.860-594G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417240 | |||||||
chr1:17417307 | C | G | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.860-661G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417307 | |||||||
chr1:17417358 | C | G | 13 | a0001c0001t0001g0058 a0001c0001t0001g0075 a0001c0001t0001g0077 others(10): Show |
13 | HG00280.hp2 HG01943.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.860-712G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417358 | |||||||
chr1:17417400 | G | T | 1 | a0001c0001t0003g0262 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.860-754C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417400 | |||||||
chr1:17417692 | A | C | 1 | a0001c0001t0029g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.860-1046T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417692 | |||||||
chr1:17417733 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.860-1087G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417733 | |||||||
chr1:17417916 | A | G | 4 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0309 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-1270T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17417916 | |||||||
chr1:17418035 | A | AT | 98 | a0001c0001t0001g0199 a0001c0001t0008g0172 a0001c0001t0008g0200 others(95): Show |
120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.860-1390dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418035 | |||||||
chr1:17418040 | A | G | 98 | a0001c0001t0001g0199 a0001c0001t0008g0172 a0001c0001t0008g0200 others(95): Show |
120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.860-1394T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418040 | |||||||
chr1:17418159 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.860-1513G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418159 | |||||||
chr1:17418213 | A | AT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0064 others(6): Show |
9 | HG00323.hp2 HG00423.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-1568dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | |||||||
chr1:17418213 | A | ATT | 25 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0014 others(22): Show |
33 | HG00558.hp2 HG00733.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.860-1569_860-1568d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | |||||||
chr1:17418213 | A | G | 1 | a0001c0002t0002g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.860-1567T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | |||||||
chr1:17418213 | AT | A | 92 | a0001c0001t0001g0058 a0001c0001t0001g0113 a0001c0001t0001g0114 others(89): Show |
113 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.860-1568delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | |||||||
chr1:17418213 | ATT | A | 7 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0154 others(4): Show |
9 | HG00738.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.860-1569_860-1568d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418213 | |||||||
chr1:17418269 | C | T | 1 | a0001c0002t0002g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.860-1623G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418269 | |||||||
chr1:17418323 | T | C | 1 | a0003c0006t0003g0205 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.860-1677A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418323 | |||||||
chr1:17418356 | G | A | 206 | a0001c0001t0001g0199 a0001c0001t0001g0213 a0001c0001t0003g0005 others(203): Show |
251 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.860-1710C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418356 | |||||||
chr1:17418390 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.860-1744C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418390 | |||||||
chr1:17418441 | G | A | 1 | a0001c0001t0004g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.860-1795C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418441 | |||||||
chr1:17418581 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.860-1935G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418581 | |||||||
chr1:17418719 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859+1995C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418719 | |||||||
chr1:17418741 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.859+1973T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418741 | |||||||
chr1:17418812 | G | A | 5 | a0001c0002t0002g0155 a0001c0002t0002g0156 a0001c0002t0002g0157 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+1902C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418812 | |||||||
chr1:17418918 | A | T | 1 | a0004c0008t0002g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.859+1796T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17418918 | |||||||
chr1:17419223 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859+1491C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419223 | |||||||
chr1:17419321 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.859+1393A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419321 | |||||||
chr1:17419353 | C | T | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.859+1361G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419353 | |||||||
chr1:17419537 | A | C | 10 | a0002c0003t0004g0283 a0002c0003t0004g0284 a0002c0003t0004g0286 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.859+1177T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419537 | |||||||
chr1:17419580 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.859+1134C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419580 | |||||||
chr1:17419772 | C | CGGACTGC others(6): Show |
1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.859+941_859+942ins others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419772 | |||||||
chr1:17419777 | C | T | 93 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(90): Show |
115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.859+937G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419777 | |||||||
chr1:17419828 | GTCTCGGG others(35): Show |
G | 1 | a0001c0001t0004g0251 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.859+844_859+885del others(42): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419828 | |||||||
chr1:17419844 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.859+870G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419844 | |||||||
chr1:17419908 | G | T | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.859+806C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17419908 | |||||||
chr1:17420028 | A | G | 1 | a0001c0001t0004g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.859+686T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420028 | |||||||
chr1:17420051 | G | A | 1 | a0001c0002t0032g0175 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.859+663C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420051 | |||||||
chr1:17420069 | G | A | 1 | a0002c0003t0006g0290 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.859+645C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420069 | |||||||
chr1:17420086 | G | A | 2 | a0001c0002t0002g0022 a0001c0002t0002g0174 |
3 | HG00323.hp1 HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.859+628C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420086 | |||||||
chr1:17420192 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0082 |
2 | HG01070.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.859+522A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420192 | |||||||
chr1:17420339 | A | G | 1 | a0001c0001t0004g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.859+375T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420339 | |||||||
chr1:17420346 | T | C | 1 | a0001c0001t0007g0275 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.859+368A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420346 | |||||||
chr1:17420580 | C | T | 1 | a0001c0001t0028g0252 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.859+134G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 7/12 | chr1 | 17420580 | |||||||
chr1:17421014 | C | G | 1 | a0001c0002t0002g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.745-186G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421014 | |||||||
chr1:17421223 | T | C | 1 | a0001c0001t0003g0229 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.745-395A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421223 | |||||||
chr1:17421230 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.745-402G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421230 | |||||||
chr1:17421231 | G | A | 1 | a0001c0001t0029g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.745-403C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421231 | |||||||
chr1:17421244 | C | A | 1 | a0004c0008t0002g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.745-416G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421244 | |||||||
chr1:17421314 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-486C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421314 | |||||||
chr1:17421452 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.745-624C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421452 | |||||||
chr1:17421472 | C | A | 1 | a0001c0001t0007g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.745-644G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421472 | |||||||
chr1:17421480 | C | T | 1 | a0005c0010t0003g0323 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.745-652G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421480 | |||||||
chr1:17421481 | G | A | 2 | a0001c0001t0004g0013 a0001c0001t0004g0254 |
4 | HG02280.hp2 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-653C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421481 | |||||||
chr1:17421496 | C | G | 2 | a0001c0001t0004g0270 a0001c0001t0004g0280 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.745-668G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421496 | |||||||
chr1:17421531 | A | G | 208 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(205): Show |
253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.744+672T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421531 | |||||||
chr1:17421692 | G | A | 4 | a0001c0001t0004g0013 a0001c0001t0004g0253 a0001c0001t0004g0254 others(1): Show |
6 | HG00738.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+511C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421692 | |||||||
chr1:17421774 | C | T | 1 | a0001c0004t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.744+429G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421774 | |||||||
chr1:17421792 | G | A | 85 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(82): Show |
106 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.744+411C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421792 | |||||||
chr1:17421931 | C | A | 208 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(205): Show |
253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.744+272G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421931 | |||||||
chr1:17421935 | G | A | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.744+268C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17421935 | |||||||
chr1:17422019 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.744+184G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422019 | |||||||
chr1:17422059 | A | C | 1 | a0001c0002t0002g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.744+144T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422059 | |||||||
chr1:17422171 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.744+32T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 6/12 | chr1 | 17422171 | |||||||
chr1:17422389 | T | C | 1 | a0001c0002t0002g0023 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.656-98A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422389 | |||||||
chr1:17422407 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.656-116C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422407 | |||||||
chr1:17422635 | C | A | 2 | a0001c0002t0002g0307 a0001c0002t0002g0308 |
2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.655+70G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 5/12 | chr1 | 17422635 | |||||||
chr1:17422963 | C | CCAA | 323 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(320): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.524-130_524-128dup others(3): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17422963 | |||||||
chr1:17423007 | C | A | 4 | a0001c0001t0004g0027 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
5 | HG01243.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-171G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423007 | |||||||
chr1:17423008 | G | A | 93 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(90): Show |
115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.524-172C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423008 | |||||||
chr1:17423061 | G | A | 3 | a0001c0001t0001g0052 a0001c0002t0012g0325 a0001c0002t0020g0299 |
3 | HG00423.hp2 HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.524-225C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423061 | |||||||
chr1:17423081 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.524-245G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423081 | |||||||
chr1:17423139 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0038 others(10): Show |
16 | HG00741.hp2 HG01928.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.524-303T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423139 | |||||||
chr1:17423152 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.524-316G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423152 | |||||||
chr1:17423285 | G | C | 3 | a0001c0001t0009g0029 a0001c0001t0009g0030 a0001c0001t0009g0238 |
5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.524-449C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423285 | |||||||
chr1:17423545 | C | T | 1 | a0001c0002t0033g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524-709G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423545 | |||||||
chr1:17423548 | C | A | 2 | a0001c0001t0003g0309 a0001c0001t0010g0233 |
2 | HG00639.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.524-712G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423548 | |||||||
chr1:17423682 | G | A | 1 | a0001c0002t0002g0151 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.524-846C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423682 | |||||||
chr1:17423767 | G | C | 4 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0309 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-931C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423767 | |||||||
chr1:17423863 | T | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.524-1027A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17423863 | |||||||
chr1:17424056 | T | C | 209 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(206): Show |
254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.524-1220A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424056 | |||||||
chr1:17424056 | T | G | 1 | a0001c0001t0031g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.524-1220A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424056 | |||||||
chr1:17424077 | G | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.524-1241C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424077 | |||||||
chr1:17424189 | G | A | 93 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(90): Show |
115 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.523+1352C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424189 | |||||||
chr1:17424274 | G | A | 1 | a0001c0001t0007g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.523+1267C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424274 | |||||||
chr1:17424368 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0131 |
3 | HG02809.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.523+1173C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424368 | |||||||
chr1:17424761 | G | A | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.523+780C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424761 | |||||||
chr1:17424875 | C | T | 2 | a0001c0002t0012g0325 a0001c0002t0020g0299 |
2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.523+666G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424875 | |||||||
chr1:17424967 | C | G | 2 | a0001c0002t0011g0201 a0001c0002t0011g0202 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.523+574G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17424967 | |||||||
chr1:17425014 | G | A | 1 | a0001c0001t0004g0242 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.523+527C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425014 | |||||||
chr1:17425108 | T | G | 1 | a0001c0001t0016g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.523+433A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425108 | |||||||
chr1:17425137 | T | C | 1 | a0001c0001t0004g0255 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.523+404A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425137 | |||||||
chr1:17425212 | G | A | 3 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0002g0308 |
3 | HG01074.hp2 HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523+329C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425212 | |||||||
chr1:17425361 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.523+180A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425361 | |||||||
chr1:17425449 | C | T | 1 | a0001c0002t0002g0025 | 2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.523+92G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425449 | |||||||
chr1:17425458 | T | C | 1 | a0001c0002t0002g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.523+83A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425458 | |||||||
chr1:17425467 | A | C | 2 | a0001c0001t0004g0014 a0001c0001t0004g0267 |
4 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+74T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425467 | |||||||
chr1:17425504 | A | G | 88 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(85): Show |
110 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.523+37T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 4/12 | chr1 | 17425504 | |||||||
chr1:17425716 | C | G | 1 | a0001c0001t0003g0221 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.380-32G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425716 | |||||||
chr1:17425771 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-87G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425771 | |||||||
chr1:17425955 | C | G | 110 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(107): Show |
133 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.380-271G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425955 | |||||||
chr1:17425992 | C | T | 3 | a0001c0001t0008g0312 a0001c0001t0008g0315 a0001c0001t0008g0316 |
3 | HG02897.hp1 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.380-308G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425992 | |||||||
chr1:17425995 | G | A | 2 | a0001c0002t0005g0177 a0001c0002t0032g0175 |
2 | HG01175.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.380-311C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17425995 | |||||||
chr1:17426011 | C | T | 1 | a0001c0002t0005g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.380-327G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426011 | |||||||
chr1:17426019 | C | T | 3 | a0001c0002t0002g0306 a0001c0002t0002g0307 a0001c0002t0002g0308 |
3 | HG01074.hp2 HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.380-335G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426019 | |||||||
chr1:17426100 | C | G | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.380-416G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426100 | |||||||
chr1:17426102 | GACCCAGG others(11): Show |
G | 1 | a0001c0001t0003g0054 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.380-436_380-419del others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426102 | |||||||
chr1:17426108 | G | A | 7 | a0001c0001t0006g0314 a0001c0001t0008g0311 a0001c0001t0008g0312 others(4): Show |
7 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.380-424C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426108 | |||||||
chr1:17426205 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380-521A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426205 | |||||||
chr1:17426235 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-551C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426235 | |||||||
chr1:17426294 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.380-610C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426294 | |||||||
chr1:17426330 | C | T | 1 | a0001c0002t0002g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.380-646G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426330 | |||||||
chr1:17426377 | A | C | 209 | a0001c0001t0001g0072 a0001c0001t0001g0186 a0001c0001t0001g0195 others(206): Show |
254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.380-693T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426377 | |||||||
chr1:17426494 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.380-810C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426494 | |||||||
chr1:17426695 | T | C | 209 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(206): Show |
254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.380-1011A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426695 | |||||||
chr1:17426753 | A | T | 1 | a0001c0001t0007g0310 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.380-1069T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426753 | |||||||
chr1:17426759 | C | CT | 16 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0055 others(13): Show |
16 | HG00423.hp2 HG00735.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.380-1076dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CT | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0117 others(18): Show |
21 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.380-1076delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CTT | C | 68 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0011 others(65): Show |
87 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.380-1077_380-1076d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CTTT | C | 35 | a0001c0001t0001g0213 a0001c0001t0003g0234 a0001c0001t0003g0235 others(32): Show |
40 | HG00558.hp2 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.380-1078_380-1076d others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0002g0161 a0001c0002t0002g0319 |
2 | HG03195.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.380-1087_380-1076d others(14): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CTTTTTTT others(6): Show |
C | 81 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(78): Show |
102 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.380-1088_380-1076d others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426759 | CTTTTTTT others(7): Show |
C | 2 | a0001c0002t0002g0158 a0001c0002t0002g0189 |
2 | HG03041.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.380-1089_380-1076d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426759 | |||||||
chr1:17426763 | T | C | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.380-1079A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426763 | |||||||
chr1:17426766 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0079 |
2 | HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.380-1082A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426766 | |||||||
chr1:17426812 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.380-1128C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426812 | |||||||
chr1:17426844 | C | A | 86 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(83): Show |
107 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.380-1160G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17426844 | |||||||
chr1:17427077 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.380-1393A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427077 | |||||||
chr1:17427143 | G | A | 102 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(99): Show |
124 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.380-1459C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427143 | |||||||
chr1:17427221 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.380-1537C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427221 | |||||||
chr1:17427253 | C | T | 87 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(84): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.380-1569G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427253 | |||||||
chr1:17427328 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.380-1644C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427328 | |||||||
chr1:17427343 | G | A | 1 | a0001c0001t0004g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.380-1659C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427343 | |||||||
chr1:17427421 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379+1685C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427421 | |||||||
chr1:17427462 | T | TTAAAACT others(7): Show |
1 | a0001c0001t0003g0054 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.379+1630_379+1643d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427462 | |||||||
chr1:17427598 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.379+1508A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427598 | |||||||
chr1:17427618 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.379+1488C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427618 | |||||||
chr1:17427732 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.379+1374G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427732 | |||||||
chr1:17427761 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.379+1345A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427761 | |||||||
chr1:17427883 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1223A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427883 | |||||||
chr1:17427884 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1222C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427884 | |||||||
chr1:17427885 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.379+1221G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427885 | |||||||
chr1:17427894 | T | A | 1 | a0001c0012t0002g0279 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.379+1212A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427894 | |||||||
chr1:17427972 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | NA19003.hp1 NA19067.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.379+1134C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17427972 | |||||||
chr1:17428035 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.379+1071A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428035 | |||||||
chr1:17428038 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0317 |
3 | HG00642.hp2 HG01261.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.379+1068C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428038 | |||||||
chr1:17428112 | T | A | 10 | a0002c0003t0004g0283 a0002c0003t0004g0284 a0002c0003t0004g0286 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.379+994A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428112 | |||||||
chr1:17428112 | T | G | 102 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(99): Show |
124 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.379+994A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428112 | |||||||
chr1:17428198 | A | G | 2 | a0001c0002t0002g0307 a0001c0002t0002g0308 |
2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.379+908T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428198 | |||||||
chr1:17428234 | A | G | 1 | a0001c0009t0001g0076 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.379+872T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428234 | |||||||
chr1:17428271 | A | C | 210 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(207): Show |
255 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.379+835T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428271 | |||||||
chr1:17428319 | G | A | 112 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0199 others(109): Show |
135 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(132): Show |
intron_variant | MODIFIER | c.379+787C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428319 | |||||||
chr1:17428336 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.379+770G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428336 | |||||||
chr1:17428420 | CCT | C | 95 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(92): Show |
117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.379+684_379+685del others(2): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428420 | |||||||
chr1:17428551 | C | T | 1 | a0001c0002t0002g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.379+555G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428551 | |||||||
chr1:17428625 | A | G | 1 | a0001c0001t0031g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379+481T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428625 | |||||||
chr1:17428919 | C | A | 6 | a0001c0001t0006g0314 a0001c0001t0008g0311 a0001c0001t0008g0312 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.379+187G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 3/12 | chr1 | 17428919 | |||||||
chr1:17429211 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-12C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429211 | |||||||
chr1:17429304 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-105G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429304 | |||||||
chr1:17429483 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.286-284T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429483 | |||||||
chr1:17429504 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.286-305C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429504 | |||||||
chr1:17429522 | G | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-323C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429522 | |||||||
chr1:17429566 | G | C | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-367C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429566 | |||||||
chr1:17429613 | C | T | 5 | a0001c0002t0002g0178 a0001c0002t0002g0179 a0001c0002t0002g0181 others(2): Show |
5 | NA18949.hp1 NA19011.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-414G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429613 | |||||||
chr1:17429694 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.286-495G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429694 | |||||||
chr1:17429715 | T | G | 1 | a0002c0005t0006g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.286-516A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429715 | |||||||
chr1:17429780 | G | A | 5 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0295 others(2): Show |
7 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-581C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429780 | |||||||
chr1:17429972 | G | A | 1 | a0001c0002t0002g0176 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.286-773C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17429972 | |||||||
chr1:17430074 | G | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-875C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430074 | |||||||
chr1:17430204 | T | C | 3 | a0001c0001t0009g0029 a0001c0001t0009g0030 a0001c0001t0009g0238 |
5 | HG01069.hp2 HG01071.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-1005A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430204 | |||||||
chr1:17430488 | C | CA | 109 | a0001c0001t0001g0072 a0001c0001t0001g0160 a0001c0001t0001g0186 others(106): Show |
131 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.286-1290dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430488 | |||||||
chr1:17430488 | C | CAA | 13 | a0001c0001t0001g0121 a0001c0002t0002g0282 a0001c0002t0005g0177 others(10): Show |
14 | HG01099.hp1 HG01106.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-1291_286-1290d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430488 | |||||||
chr1:17430502 | A | G | 1 | a0001c0001t0003g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.286-1303T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430502 | |||||||
chr1:17430720 | G | A | 95 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(92): Show |
117 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.286-1521C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430720 | |||||||
chr1:17430725 | T | G | 98 | a0001c0001t0001g0072 a0001c0001t0001g0160 a0001c0001t0001g0186 others(95): Show |
120 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(117): Show |
intron_variant | MODIFIER | c.286-1526A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430725 | |||||||
chr1:17430790 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.286-1591C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430790 | |||||||
chr1:17430970 | G | A | 2 | a0001c0002t0002g0307 a0001c0002t0002g0308 |
2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.286-1771C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17430970 | |||||||
chr1:17431025 | A | G | 1 | a0001c0001t0008g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-1826T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431025 | |||||||
chr1:17431095 | C | T | 1 | a0001c0001t0008g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-1896G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431095 | |||||||
chr1:17431103 | C | T | 4 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0295 others(1): Show |
6 | HG02559.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-1904G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431103 | |||||||
chr1:17431333 | C | CA | 13 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0001g0082 others(10): Show |
14 | HG00099.hp2 HG01070.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.286-2135dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | |||||||
chr1:17431333 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0007g0274 a0001c0001t0007g0275 a0001c0012t0002g0279 |
3 | HG01361.hp2 HG01496.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.286-2135_286-2134i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | |||||||
chr1:17431333 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0007g0278 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.286-2135_286-2134i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | |||||||
chr1:17431333 | CA | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0038 others(11): Show |
17 | HG00423.hp2 HG00741.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.286-2135delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431333 | |||||||
chr1:17431334 | A | AAAAAAAA others(9): Show |
4 | a0001c0001t0007g0273 a0001c0001t0007g0276 a0001c0001t0007g0277 others(1): Show |
4 | HG03486.hp1 NA18962.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2136_286-2135i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431334 | |||||||
chr1:17431343 | A | T | 86 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(83): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-2144T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431343 | |||||||
chr1:17431345 | A | T | 1 | a0001c0002t0002g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.286-2146T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431345 | |||||||
chr1:17431350 | A | T | 86 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(83): Show |
108 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-2151T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431350 | |||||||
chr1:17431350 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.286-2162_286-2152d others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431350 | |||||||
chr1:17431355 | A | AATATATA others(3): Show |
1 | a0001c0002t0002g0298 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.286-2157_286-2156i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | |||||||
chr1:17431355 | A | AATATATA others(13): Show |
1 | a0001c0001t0008g0312 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.286-2157_286-2156i others(22): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | |||||||
chr1:17431355 | A | ATATATAT others(6): Show |
1 | a0001c0002t0002g0297 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286-2157_286-2156i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | |||||||
chr1:17431355 | A | T | 2 | a0001c0001t0031g0037 a0001c0002t0002g0217 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.286-2156T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431355 | |||||||
chr1:17431356 | AAAAATAT | A | 7 | a0002c0003t0004g0284 a0002c0003t0006g0032 a0002c0003t0006g0287 others(4): Show |
8 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2164_286-2158d others(9): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431356 | |||||||
chr1:17431357 | A | AATATATA others(3): Show |
1 | a0001c0004t0004g0035 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | |||||||
chr1:17431357 | A | AATATATA others(33): Show |
1 | a0001c0002t0002g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(42): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | |||||||
chr1:17431357 | A | ATATATAT others(24): Show |
1 | a0001c0001t0010g0224 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.286-2159_286-2158i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | |||||||
chr1:17431357 | A | T | 6 | a0001c0001t0008g0312 a0001c0001t0031g0037 a0001c0002t0002g0297 others(3): Show |
6 | HG02622.hp2 HG02809.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2158T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431357 | |||||||
chr1:17431359 | A | AAAAAAAA others(14): Show |
1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAA others(52): Show |
1 | a0001c0001t0001g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(61): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0008g0172 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAA others(17): Show |
1 | a0001c0002t0002g0171 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(26): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAA others(39): Show |
1 | a0001c0002t0002g0022 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(48): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAT others(8): Show |
1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAAAT others(40): Show |
1 | a0001c0002t0002g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(49): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAATA others(3): Show |
1 | a0001c0002t0002g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAATA others(9): Show |
1 | a0001c0002t0002g0033 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAATA others(15): Show |
1 | a0001c0002t0002g0169 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(24): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAATA others(19): Show |
2 | a0001c0002t0002g0176 a0001c0002t0002g0193 |
2 | HG02080.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(28): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAAATA others(39): Show |
1 | a0001c0002t0002g0143 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(48): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0008g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(6): Show |
2 | a0001c0002t0002g0296 a0001c0002t0005g0021 |
2 | HG01433.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(14): Show |
1 | a0001c0001t0008g0311 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(16): Show |
1 | a0001c0002t0002g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(18): Show |
4 | a0001c0002t0002g0020 a0001c0002t0002g0023 a0001c0002t0005g0165 others(1): Show |
4 | HG00735.hp1 HG02004.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(20): Show |
2 | a0001c0002t0002g0023 a0001c0002t0002g0194 |
2 | HG01255.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(24): Show |
2 | a0001c0002t0002g0151 a0001c0002t0005g0021 |
2 | HG02015.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(34): Show |
1 | a0001c0002t0002g0154 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(43): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(36): Show |
1 | a0001c0002t0002g0152 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAAATAT others(44): Show |
1 | a0001c0002t0005g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(53): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(3): Show |
2 | a0001c0002t0002g0148 a0001c0002t0002g0306 |
2 | HG01074.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(12): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(5): Show |
3 | a0001c0002t0002g0033 a0001c0002t0002g0034 a0001c0002t0002g0295 |
3 | HG02559.hp1 HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(14): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(7): Show |
1 | a0001c0002t0002g0159 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(9): Show |
2 | a0001c0002t0012g0325 a0001c0002t0020g0299 |
2 | HG00642.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(18): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(11): Show |
2 | a0001c0002t0002g0157 a0001c0002t0002g0303 |
2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(13): Show |
1 | a0001c0002t0002g0163 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(22): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(15): Show |
1 | a0001c0002t0002g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(24): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(17): Show |
1 | a0001c0002t0002g0302 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(26): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(23): Show |
2 | a0001c0002t0002g0004 a0001c0002t0002g0025 |
2 | HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(32): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(25): Show |
2 | a0001c0002t0002g0004 a0001c0002t0002g0164 |
2 | HG01123.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(34): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(27): Show |
1 | a0001c0002t0002g0191 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(36): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(29): Show |
1 | a0001c0002t0002g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(38): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAAATATA others(31): Show |
1 | a0001c0002t0002g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(40): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(4): Show |
2 | a0001c0002t0002g0034 a0001c0002t0002g0294 |
2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(8): Show |
1 | a0001c0002t0002g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(10): Show |
1 | a0001c0002t0002g0161 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(12): Show |
2 | a0001c0001t0006g0314 a0001c0001t0017g0313 |
2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(14): Show |
1 | a0001c0001t0008g0316 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(16): Show |
1 | a0001c0001t0008g0315 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(24): Show |
1 | a0001c0002t0002g0020 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AAATATAT others(28): Show |
1 | a0001c0002t0002g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AATATATA others(7): Show |
1 | a0001c0002t0002g0304 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.286-2174_286-2161d others(16): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AATATATA others(11): Show |
1 | a0001c0002t0002g0155 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.286-2178_286-2161d others(20): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | AATATATA others(23): Show |
2 | a0001c0002t0002g0004 a0001c0002t0002g0025 |
2 | HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(32): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(18): Show |
1 | a0001c0001t0003g0012 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(20): Show |
1 | a0001c0001t0004g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(36): Show |
1 | a0001c0001t0014g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(42): Show |
1 | a0001c0001t0014g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(51): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(26): Show |
4 | a0001c0001t0003g0011 a0001c0001t0003g0232 a0001c0001t0003g0272 others(1): Show |
4 | HG00099.hp1 HG02040.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(35): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(28): Show |
1 | a0001c0001t0004g0244 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAA others(36): Show |
1 | a0001c0001t0003g0322 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(4): Show |
3 | a0001c0001t0001g0213 a0001c0001t0004g0204 a0001c0001t0004g0212 |
3 | HG02735.hp2 HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(13): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(6): Show |
1 | a0001c0001t0003g0324 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(15): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(8): Show |
4 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0264 others(1): Show |
4 | HG02895.hp2 NA19005.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(10): Show |
3 | a0001c0001t0003g0241 a0001c0001t0004g0014 a0001c0001t0004g0208 |
3 | HG02602.hp2 HG03942.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(19): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(12): Show |
1 | a0001c0001t0004g0007 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(14): Show |
3 | a0001c0001t0009g0029 a0001c0001t0009g0030 a0001c0001t0034g0207 |
4 | HG00639.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(16): Show |
3 | a0001c0001t0004g0027 a0001c0001t0004g0210 a0001c0001t0004g0248 |
4 | HG01243.hp1 HG01978.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(25): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(18): Show |
9 | a0001c0001t0003g0005 a0001c0001t0003g0225 a0001c0001t0003g0261 others(6): Show |
9 | HG00438.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(27): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(20): Show |
8 | a0001c0001t0003g0005 a0001c0001t0003g0028 a0001c0001t0003g0214 others(5): Show |
8 | HG02165.hp1 NA18940.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(22): Show |
6 | a0001c0001t0003g0006 a0001c0001t0003g0031 a0001c0001t0003g0054 others(3): Show |
6 | HG00558.hp1 HG00609.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(31): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(24): Show |
5 | a0001c0001t0003g0006 a0001c0001t0003g0218 a0001c0001t0004g0013 others(2): Show |
6 | HG02886.hp2 HG03486.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(33): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(26): Show |
7 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0228 others(4): Show |
7 | HG00673.hp2 HG02071.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(35): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(28): Show |
12 | a0001c0001t0003g0031 a0001c0001t0003g0220 a0001c0001t0003g0231 others(9): Show |
12 | HG00423.hp1 HG00738.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(37): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(30): Show |
4 | a0001c0001t0003g0216 a0001c0001t0003g0229 a0001c0001t0003g0230 others(1): Show |
4 | NA18949.hp2 NA18952.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(39): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(32): Show |
5 | a0001c0001t0003g0005 a0001c0001t0003g0011 a0001c0001t0003g0012 others(2): Show |
5 | HG02132.hp2 NA18747.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(41): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(34): Show |
4 | a0001c0001t0003g0321 a0001c0001t0004g0007 a0001c0001t0004g0266 others(1): Show |
4 | HG00323.hp2 HG00639.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(43): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(36): Show |
2 | a0001c0001t0004g0254 a0003c0006t0003g0205 |
2 | HG02647.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(45): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(38): Show |
3 | a0001c0001t0003g0053 a0001c0001t0003g0309 a0001c0001t0004g0243 |
3 | HG03831.hp2 NA19082.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(47): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(40): Show |
4 | a0001c0001t0004g0242 a0001c0001t0004g0250 a0001c0001t0004g0255 others(1): Show |
4 | HG00558.hp2 HG02040.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(49): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAAAAT others(62): Show |
1 | a0001c0001t0004g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(71): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAATAT others(14): Show |
2 | a0001c0001t0009g0030 a0001c0001t0009g0238 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.286-2161_286-2160i others(23): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAAATAT others(20): Show |
1 | a0001c0001t0003g0215 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.286-2161_286-2160i others(29): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATAT | 6 | a0001c0001t0007g0274 a0001c0001t0007g0275 a0001c0001t0007g0276 others(3): Show |
6 | HG01496.hp1 NA18962.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2161_286-2160i others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | ATATATAT others(8): Show |
1 | a0001c0002t0033g0300 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.286-2161_286-2160i others(17): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | A | T | 8 | a0001c0001t0008g0312 a0001c0001t0010g0224 a0001c0001t0031g0037 others(5): Show |
9 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-2160T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431359 | AAT | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0055 others(33): Show |
43 | HG00140.hp2 HG01071.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.286-2162_286-2161d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431359 | |||||||
chr1:17431360 | AT | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(51): Show |
64 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.286-2162delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431360 | |||||||
chr1:17431361 | T | A | 18 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0069 others(15): Show |
18 | HG01123.hp2 HG02148.hp1 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.286-2162A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431361 | |||||||
chr1:17431363 | T | A | 22 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0002t0002g0001 others(19): Show |
30 | HG00140.hp2 HG01071.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.286-2164A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431363 | |||||||
chr1:17431365 | T | A | 2 | a0001c0002t0002g0196 a0001c0002t0002g0197 |
2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.286-2166A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431365 | |||||||
chr1:17431367 | T | A | 2 | a0001c0001t0003g0239 a0001c0002t0002g0197 |
2 | HG00438.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.286-2168A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431367 | |||||||
chr1:17431369 | T | A | 1 | a0001c0001t0003g0239 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.286-2170A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431369 | |||||||
chr1:17431424 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2225A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431424 | |||||||
chr1:17431441 | C | T | 87 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(84): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.286-2242G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431441 | |||||||
chr1:17431491 | C | A | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-2292G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431491 | |||||||
chr1:17431499 | C | CA | 22 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0073 others(19): Show |
22 | HG01099.hp2 HG01106.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.286-2301dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | |||||||
chr1:17431499 | C | CAA | 84 | a0001c0001t0001g0072 a0001c0001t0001g0160 a0001c0001t0001g0186 others(81): Show |
105 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.286-2302_286-2301d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | |||||||
chr1:17431499 | C | CAAA | 7 | a0001c0002t0002g0157 a0001c0002t0002g0158 a0001c0002t0002g0193 others(4): Show |
8 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.286-2303_286-2301d others(5): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | |||||||
chr1:17431499 | CA | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0077 others(16): Show |
20 | HG01070.hp1 HG01361.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.286-2301delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | |||||||
chr1:17431499 | CAA | C | 84 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(81): Show |
106 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.286-2302_286-2301d others(4): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431499 | |||||||
chr1:17431553 | A | G | 5 | a0001c0002t0002g0155 a0001c0002t0002g0156 a0001c0002t0002g0157 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-2354T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431553 | |||||||
chr1:17431579 | T | C | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-2380A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431579 | |||||||
chr1:17431582 | G | C | 2 | a0001c0002t0002g0144 a0001c0002t0002g0145 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.286-2383C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431582 | |||||||
chr1:17431694 | T | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.286-2495A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431694 | |||||||
chr1:17431700 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.286-2501G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17431700 | |||||||
chr1:17432132 | C | T | 1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.286-2933G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432132 | |||||||
chr1:17432164 | T | C | 29 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0014 others(26): Show |
37 | HG00323.hp2 HG00558.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.286-2965A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432164 | |||||||
chr1:17432296 | T | C | 1 | a0001c0001t0004g0258 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.286-3097A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432296 | |||||||
chr1:17432324 | C | T | 1 | a0001c0001t0003g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.286-3125G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432324 | |||||||
chr1:17432577 | C | T | 5 | a0001c0002t0002g0155 a0001c0002t0002g0156 a0001c0002t0002g0157 others(2): Show |
5 | HG02109.hp1 HG02258.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-3378G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432577 | |||||||
chr1:17432717 | T | C | 1 | a0001c0002t0002g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286-3518A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432717 | |||||||
chr1:17432749 | T | C | 212 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0160 others(209): Show |
257 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.286-3550A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432749 | |||||||
chr1:17432850 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.286-3651G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432850 | |||||||
chr1:17432851 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | NA19003.hp1 NA19067.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-3652C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432851 | |||||||
chr1:17432858 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.286-3659A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432858 | |||||||
chr1:17432890 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.286-3691C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432890 | |||||||
chr1:17432907 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.286-3708C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432907 | |||||||
chr1:17432959 | AAAAAAG | A | 19 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0002t0002g0001 others(16): Show |
26 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.286-3766_286-3761d others(8): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432959 | |||||||
chr1:17432991 | T | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0054 |
3 | HG00423.hp1 NA19086.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.286-3792A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17432991 | |||||||
chr1:17433021 | T | C | 3 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0145 |
3 | HG01256.hp1 HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.286-3822A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433021 | |||||||
chr1:17433040 | A | G | 2 | a0001c0004t0004g0035 a0001c0004t0004g0305 |
3 | HG02622.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.286-3841T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433040 | |||||||
chr1:17433397 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.286-4198C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433397 | |||||||
chr1:17433398 | C | G | 10 | a0002c0003t0004g0283 a0002c0003t0004g0284 a0002c0003t0004g0286 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.286-4199G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433398 | |||||||
chr1:17433423 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.286-4224G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433423 | |||||||
chr1:17433449 | T | C | 1 | a0001c0001t0006g0203 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.286-4250A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433449 | |||||||
chr1:17433485 | C | T | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.286-4286G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433485 | |||||||
chr1:17433519 | G | GT | 5 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 others(2): Show |
5 | HG02559.hp1 HG04204.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-4321dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433519 | |||||||
chr1:17433524 | T | G | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4325A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433524 | |||||||
chr1:17433525 | T | G | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4326A>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433525 | |||||||
chr1:17433526 | T | A | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4327A>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433526 | |||||||
chr1:17433527 | G | C | 1 | a0001c0002t0002g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.286-4328C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433527 | |||||||
chr1:17433549 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.286-4350G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433549 | |||||||
chr1:17433602 | A | G | 87 | a0001c0001t0001g0072 a0001c0001t0001g0160 a0001c0001t0001g0186 others(84): Show |
108 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.286-4403T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433602 | |||||||
chr1:17433662 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.286-4463G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433662 | |||||||
chr1:17433833 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.285+4397G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433833 | |||||||
chr1:17433836 | G | T | 1 | a0001c0002t0002g0294 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+4394C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433836 | |||||||
chr1:17433837 | GAGGTA | G | 5 | a0001c0002t0002g0020 a0001c0002t0002g0151 a0001c0002t0002g0152 others(2): Show |
6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4388_285+4392d others(7): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433837 | |||||||
chr1:17433843 | A | T | 5 | a0001c0002t0002g0020 a0001c0002t0002g0151 a0001c0002t0002g0152 others(2): Show |
6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4387T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433843 | |||||||
chr1:17433844 | G | C | 5 | a0001c0002t0002g0020 a0001c0002t0002g0151 a0001c0002t0002g0152 others(2): Show |
6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4386C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433844 | |||||||
chr1:17433845 | A | T | 5 | a0001c0002t0002g0020 a0001c0002t0002g0151 a0001c0002t0002g0152 others(2): Show |
6 | HG02015.hp2 HG02080.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+4385T>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433845 | |||||||
chr1:17433848 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+4382G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433848 | |||||||
chr1:17433936 | T | C | 32 | a0001c0001t0004g0007 a0001c0001t0004g0013 a0001c0001t0004g0014 others(29): Show |
40 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.285+4294A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17433936 | |||||||
chr1:17434417 | C | G | 1 | a0001c0001t0031g0037 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.285+3813G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434417 | |||||||
chr1:17434564 | A | C | 1 | a0001c0001t0024g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+3666T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434564 | |||||||
chr1:17434614 | C | A | 7 | a0001c0001t0007g0274 a0001c0001t0007g0275 a0001c0001t0007g0276 others(4): Show |
7 | HG01361.hp2 HG01496.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3616G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434614 | |||||||
chr1:17434647 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.285+3583C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434647 | |||||||
chr1:17434839 | G | A | 13 | a0001c0001t0003g0259 a0001c0001t0003g0260 a0001c0001t0003g0261 others(10): Show |
19 | HG00438.hp2 HG01081.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.285+3391C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434839 | |||||||
chr1:17434876 | G | A | 1 | a0001c0001t0003g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.285+3354C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17434876 | |||||||
chr1:17435070 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.285+3160A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435070 | |||||||
chr1:17435206 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.285+3024G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435206 | |||||||
chr1:17435800 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.285+2430G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435800 | |||||||
chr1:17435918 | CA | C | 109 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0160 others(106): Show |
132 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.285+2311delT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17435918 | |||||||
chr1:17436085 | T | C | 10 | a0002c0003t0004g0283 a0002c0003t0004g0284 a0002c0003t0004g0286 others(7): Show |
11 | HG01099.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+2145A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436085 | |||||||
chr1:17436170 | A | C | 1 | a0001c0002t0002g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.285+2060T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436170 | |||||||
chr1:17436174 | G | A | 1 | a0001c0001t0025g0265 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.285+2056C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436174 | |||||||
chr1:17436239 | G | A | 4 | a0001c0001t0004g0014 a0001c0001t0004g0266 a0001c0001t0004g0267 others(1): Show |
6 | HG00323.hp2 HG00733.hp1 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+1991C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436239 | |||||||
chr1:17436320 | A | G | 2 | a0001c0001t0004g0270 a0001c0001t0004g0280 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.285+1910T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436320 | |||||||
chr1:17436364 | T | C | 2 | a0001c0002t0002g0307 a0001c0002t0002g0308 |
2 | HG01167.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.285+1866A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436364 | |||||||
chr1:17436397 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0004g0269 |
2 | HG02698.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.285+1833C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436397 | |||||||
chr1:17436440 | G | A | 1 | a0001c0001t0008g0200 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+1790C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436440 | |||||||
chr1:17436635 | C | A | 2 | a0001c0002t0002g0148 a0001c0002t0002g0282 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.285+1595G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436635 | |||||||
chr1:17436732 | C | A | 1 | a0002c0005t0006g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+1498G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436732 | |||||||
chr1:17436816 | A | G | 211 | a0001c0001t0001g0066 a0001c0001t0001g0160 a0001c0001t0001g0186 others(208): Show |
256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.285+1414T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436816 | |||||||
chr1:17436934 | G | A | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+1296C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436934 | |||||||
chr1:17436976 | A | G | 1 | a0001c0002t0002g0293 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.285+1254T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17436976 | |||||||
chr1:17437007 | C | T | 1 | a0001c0002t0002g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285+1223G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437007 | |||||||
chr1:17437021 | A | G | 211 | a0001c0001t0001g0066 a0001c0001t0001g0160 a0001c0001t0001g0186 others(208): Show |
256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.285+1209T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437021 | |||||||
chr1:17437070 | G | C | 113 | a0001c0001t0001g0160 a0001c0001t0001g0186 a0001c0001t0001g0195 others(110): Show |
136 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.285+1160C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437070 | |||||||
chr1:17437508 | G | T | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+722C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437508 | |||||||
chr1:17437557 | G | C | 2 | a0001c0002t0011g0201 a0001c0002t0011g0202 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.285+673C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437557 | |||||||
chr1:17437579 | C | G | 4 | a0001c0001t0004g0027 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
5 | HG01243.hp1 HG01943.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+651G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437579 | |||||||
chr1:17437580 | G | A | 1 | a0002c0005t0006g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285+650C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437580 | |||||||
chr1:17437601 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.285+629G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437601 | |||||||
chr1:17437637 | G | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.285+593C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437637 | |||||||
chr1:17437647 | C | G | 2 | a0001c0001t0004g0208 a0001c0001t0034g0207 |
2 | HG00639.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.285+583G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437647 | |||||||
chr1:17437673 | A | AGCATGCG others(72): Show |
1 | a0001c0002t0002g0319 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(79): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | |||||||
chr1:17437673 | A | AGCATGCG others(73): Show |
1 | a0001c0001t0026g0206 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(80): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | |||||||
chr1:17437673 | A | AGCATGCG others(71): Show |
2 | a0002c0003t0004g0283 a0002c0003t0004g0284 |
2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.285+556_285+557ins others(78): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | |||||||
chr1:17437673 | A | AGCATGCG others(71): Show |
1 | a0001c0001t0001g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.285+556_285+557ins others(78): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437673 | |||||||
chr1:17437745 | C | T | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285+485G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437745 | |||||||
chr1:17437753 | ACGGCCGC others(14): Show |
A | 1 | a0001c0001t0003g0271 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.285+456_285+476del others(21): Show |
RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437753 | |||||||
chr1:17437754 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.285+476G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437754 | |||||||
chr1:17437765 | C | G | 1 | a0001c0001t0004g0254 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.285+465G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437765 | |||||||
chr1:17437765 | C | T | 1 | a0001c0004t0004g0305 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+465G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437765 | |||||||
chr1:17437851 | C | G | 1 | a0001c0001t0027g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+379G>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437851 | |||||||
chr1:17437882 | C | A | 1 | a0001c0001t0003g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.285+348G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437882 | |||||||
chr1:17437912 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.285+318T>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437912 | |||||||
chr1:17437928 | C | T | 1 | a0001c0002t0005g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.285+302G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437928 | |||||||
chr1:17437976 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.285+254G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437976 | |||||||
chr1:17437985 | C | A | 1 | a0001c0001t0001g0281 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.285+245G>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17437985 | |||||||
chr1:17438008 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.285+222C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438008 | |||||||
chr1:17438044 | C | T | 1 | a0001c0002t0002g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285+186G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438044 | |||||||
chr1:17438110 | C | T | 1 | a0001c0002t0005g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.285+120G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438110 | |||||||
chr1:17438131 | G | A | 101 | a0001c0001t0001g0160 a0001c0001t0001g0186 a0001c0001t0001g0195 others(98): Show |
123 | HG00140.hp2 HG00323.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.285+99C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 2/12 | chr1 | 17438131 | |||||||
chr1:17438582 | G | T | 1 | a0001c0001t0004g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-8-60C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438582 | |||||||
chr1:17438603 | C | T | 1 | a0001c0002t0002g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-8-81G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438603 | |||||||
chr1:17438641 | G | A | 8 | a0001c0001t0007g0273 a0001c0001t0007g0274 a0001c0001t0007g0275 others(5): Show |
8 | HG01361.hp2 HG01496.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-119C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438641 | |||||||
chr1:17438644 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-122C>T | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438644 | |||||||
chr1:17438767 | G | T | 3 | a0001c0002t0005g0049 a0001c0002t0005g0050 a0001c0002t0013g0051 |
3 | HG01070.hp2 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-8-245C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438767 | |||||||
chr1:17438817 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8-295T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438817 | |||||||
chr1:17438873 | C | T | 3 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0145 |
3 | HG01256.hp1 HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-8-351G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438873 | |||||||
chr1:17438988 | T | C | 211 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0186 others(208): Show |
256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-8-466A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17438988 | |||||||
chr1:17439009 | G | C | 211 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0186 others(208): Show |
256 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.-8-487C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439009 | |||||||
chr1:17439049 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+496A>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439049 | |||||||
chr1:17439100 | G | C | 1 | a0001c0001t0006g0203 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9+445C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439100 | |||||||
chr1:17439136 | G | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+409C>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439136 | |||||||
chr1:17439184 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-9+361G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439184 | |||||||
chr1:17439260 | C | T | 97 | a0001c0001t0001g0213 a0001c0001t0003g0005 a0001c0001t0003g0006 others(94): Show |
119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.-9+285G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439260 | |||||||
chr1:17439307 | G | C | 1 | a0001c0001t0003g0309 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+238C>G | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439307 | |||||||
chr1:17439330 | C | CT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0038 others(14): Show |
20 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+214dupA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | |||||||
chr1:17439330 | CT | C | 128 | a0001c0001t0001g0213 a0001c0001t0001g0281 a0001c0001t0003g0005 others(125): Show |
154 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-9+214delA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | |||||||
chr1:17439330 | CTT | C | 7 | a0001c0001t0006g0314 a0001c0001t0007g0310 a0001c0001t0008g0311 others(4): Show |
7 | HG02280.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+213_-9+214delAA | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439330 | |||||||
chr1:17439484 | G | GA | 9 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0003g0321 others(6): Show |
9 | HG02145.hp1 HG03516.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+60dupT | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439484 | |||||||
chr1:17439488 | A | G | 1 | a0001c0001t0035g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-9+57T>C | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439488 | |||||||
chr1:17439539 | C | T | 1 | a0001c0001t0031g0037 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.-9+6G>A | RCC2 | ENSG00000179051.14 | transcript | ENST00000375436.9 | protein_coding | 1/12 | chr1 | 17439539 |