Item | Value |
---|---|
geneid | 10171 |
ensemblid | ENSG00000120158.12 |
hgncid | 17687 |
symbol | RCL1 |
name | RNA terminal phosphate cyclase like 1 |
refseq_nuc | NM_005772.5 |
refseq_prot | NP_005763.3 |
ensembl_nuc | ENST00000381750.9 |
ensembl_prot | ENSP00000371169.4 |
mane_status | MANE Select |
chr | chr9 |
start | 4792944 |
end | 4861066 |
strand | + |
ver | v1.2 |
region | chr9:4792944-4861066 |
region5000 | chr9:4787944-4866066 |
regionname0 | RCL1_chr9_4792944_4861066 |
regionname5000 | RCL1_chr9_4787944_4866066 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 373 | 380 | 91 | 67 | 160 | 16 | 44 | 128 | RCL1_chr9_4787944_4866066 | RCL1 | MATQA others(368): Show |
chr9 | 4787944 | 4866066 |
a0002 | 0/0 | 373 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | MATQA others(368): Show |
chr9 | 4787944 | 4866066 |
a0003 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | MATQA others(368): Show |
chr9 | 4787944 | 4866066 |
a0004 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | MATQA others(368): Show |
chr9 | 4787944 | 4866066 |
a0005 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | MATQA others(368): Show |
chr9 | 4787944 | 4866066 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1119 | 370 | 87 | 64 | 157 | 16 | 44 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0003 | 0/0 | 1119 | 3 | 0 | 0 | 3 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0004 | 0/0 | 1119 | 2 | 1 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0005 | 0/0 | 1119 | 2 | 1 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0007 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0008 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0001c0010 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0002c0002 | 0/0 | 1119 | 3 | 3 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0003c0006 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0004c0009 | 0/0 | 1119 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 | ||
a0005c0011 | 0/0 | 1119 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | ATGGC others(1114): Show |
chr9 | 4787944 | 4866066 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2062 | 112 | 32 | 10 | 60 | 2 | 8 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0002 | 0/1 | 2061 | 92 | 16 | 20 | 29 | 9 | 17 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0003 | 0/0 | 2062 | 50 | 7 | 16 | 22 | 2 | 3 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0004 | 0/0 | 2061 | 12 | 2 | 3 | 4 | 0 | 3 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0005 | 1/0 | 2061 | 13 | 1 | 4 | 1 | 1 | 5 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0006 | 0/0 | 2061 | 13 | 0 | 1 | 10 | 0 | 2 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0007 | 0/0 | 2062 | 10 | 0 | 5 | 5 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0008 | 0/0 | 2062 | 10 | 10 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0009 | 0/0 | 2062 | 8 | 0 | 0 | 8 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0010 | 0/0 | 2061 | 8 | 0 | 0 | 6 | 0 | 2 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0011 | 0/0 | 2062 | 5 | 2 | 2 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0012 | 0/0 | 2061 | 4 | 3 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0013 | 0/0 | 2062 | 4 | 4 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0014 | 0/0 | 2062 | 3 | 2 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0015 | 0/0 | 2062 | 3 | 1 | 0 | 0 | 2 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0016 | 0/0 | 2062 | 2 | 0 | 0 | 1 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0017 | 0/0 | 2061 | 3 | 0 | 0 | 3 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0018 | 0/0 | 2062 | 2 | 2 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0019 | 0/0 | 2062 | 2 | 0 | 0 | 2 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0020 | 0/0 | 2062 | 2 | 2 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0021 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0022 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0023 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0024 | 0/0 | 2062 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0025 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0029 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0030 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0032 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0033 | 0/0 | 2062 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0034 | 0/0 | 2062 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0001t0035 | 0/0 | 2061 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0003t0002 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0003t0016 | 0/0 | 2062 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0004t0002 | 0/0 | 2061 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0004t0027 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0005t0001 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0005t0004 | 0/0 | 2061 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0001c0007t0003 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0008t0026 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0001c0010t0001 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0002c0002t0004 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0002c0002t0014 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0002c0002t0028 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0003c0006t0036 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2056): Show |
chr9 | 4787944 | 4866066 |
a0004c0009t0001 | 0/0 | 2062 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
a0005c0011t0031 | 0/0 | 2062 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | AAACC others(2057): Show |
chr9 | 4787944 | 4866066 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0003g0377 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0004g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0008g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0010g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0011g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0011g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0012g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0012g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0012g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0013g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0013g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0014g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0014g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0015g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0015g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0016g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0016g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0017g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0018g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0019g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0019g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0021g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0021g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0022g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0023g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0024g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0029g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0030g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0032g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0033g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0034g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0001t0035g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0003t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0004t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0004t0027g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0005t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0005t0004g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0007t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0008t0026g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0001c0010t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0002c0002t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0002c0002t0014g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0002c0002t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0003c0006t0036g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0004c0009t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
a0005c0011t0031g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0075 | EUR | GBR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0377 | EUR | GBR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0219 | EUR | GBR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | FIN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | FIN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00438 | hp1 | a0001 | c0001 | t0022 | g0051 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0327 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01099 | hp1 | a0001 | c0004 | t0002 | g0004 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0353 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01106 | hp1 | a0001 | c0001 | t0011 | g0057 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0081 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01192 | hp1 | a0001 | c0005 | t0004 | g0378 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01243 | hp1 | a0001 | c0001 | t0012 | g0197 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01243 | hp2 | a0001 | c0001 | t0035 | g0277 | AMR | PUR | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0287 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01361 | hp2 | a0001 | c0001 | t0011 | g0055 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0043 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0317 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0249 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01515 | hp2 | a0001 | c0001 | t0015 | g0065 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0212 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | IBS | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01884 | hp2 | a0003 | c0006 | t0036 | g0196 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0352 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0040 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01952 | hp2 | a0004 | c0009 | t0001 | g0066 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01975 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01978 | hp1 | a0001 | c0007 | t0003 | g0238 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01981 | hp1 | a0001 | c0001 | t0014 | g0194 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0316 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02015 | hp1 | a0001 | c0001 | t0019 | g0027 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02040 | hp1 | a0001 | c0001 | t0019 | g0125 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02055 | hp1 | a0001 | c0001 | t0008 | g0202 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0361 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02074 | hp2 | a0001 | c0001 | t0029 | g0140 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02145 | hp1 | a0001 | c0001 | t0018 | g0294 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | CDX | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | CDX | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CDX | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | CDX | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0325 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02258 | hp2 | a0002 | c0002 | t0014 | g0304 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0053 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0372 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0195 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02572 | hp2 | a0001 | c0001 | t0018 | g0312 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02602 | hp2 | a0001 | c0001 | t0010 | g0224 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02622 | hp1 | a0001 | c0001 | t0030 | g0201 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0348 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02647 | hp1 | a0001 | c0001 | t0023 | g0241 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0342 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0245 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02735 | hp1 | a0001 | c0001 | t0016 | g0225 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0319 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0293 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0292 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0244 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02886 | hp1 | a0002 | c0002 | t0004 | g0198 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0351 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02922 | hp2 | a0001 | c0004 | t0027 | g0193 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0360 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02976 | hp2 | a0005 | c0011 | t0031 | g0096 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03098 | hp2 | a0001 | c0008 | t0026 | g0200 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0354 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03139 | hp1 | a0001 | c0001 | t0014 | g0368 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0344 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03195 | hp1 | a0001 | c0010 | t0001 | g0272 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0357 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0362 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03453 | hp1 | a0002 | c0002 | t0028 | g0018 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0280 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0279 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ESN | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0376 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0060 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0373 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03834 | hp1 | a0001 | c0001 | t0034 | g0102 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0289 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0341 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0286 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0380 | SAS | BEB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0379 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04204 | hp2 | a0001 | c0001 | t0032 | g0187 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0315 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0006 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18522 | hp2 | a0001 | c0001 | t0013 | g0301 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0334 | EAS | CHB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | CHB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | CHB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18939 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18942 | hp2 | a0001 | c0001 | t0009 | g0101 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18944 | hp1 | a0001 | c0003 | t0016 | g0046 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18947 | hp1 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0370 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18951 | hp2 | a0001 | c0001 | t0017 | g0033 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18953 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18954 | hp1 | a0001 | c0001 | t0016 | g0320 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18957 | hp1 | a0001 | c0001 | t0006 | g0328 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18957 | hp2 | a0001 | c0001 | t0010 | g0142 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18961 | hp1 | a0001 | c0001 | t0024 | g0329 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18963 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18964 | hp2 | a0001 | c0001 | t0017 | g0032 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0170 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18975 | hp1 | a0001 | c0001 | t0021 | g0182 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18975 | hp2 | a0001 | c0001 | t0010 | g0098 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18978 | hp1 | a0001 | c0001 | t0009 | g0094 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18979 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18983 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18990 | hp1 | a0001 | c0001 | t0009 | g0104 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18993 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18994 | hp2 | a0001 | c0001 | t0021 | g0183 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19007 | hp2 | a0001 | c0001 | t0007 | g0049 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19010 | hp1 | a0001 | c0001 | t0033 | g0184 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19011 | hp2 | a0001 | c0001 | t0007 | g0047 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19062 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19072 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19078 | hp1 | a0001 | c0001 | t0010 | g0041 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19078 | hp2 | a0001 | c0003 | t0002 | g0145 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19086 | hp1 | a0001 | c0001 | t0010 | g0144 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0179 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0375 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19091 | hp2 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19240 | hp1 | a0001 | c0001 | t0020 | g0052 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | YRI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0356 | AFR | ASW | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ASW | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20805 | hp1 | a0001 | c0001 | t0005 | g0288 | EUR | TSI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20805 | hp2 | a0001 | c0001 | t0015 | g0063 | EUR | TSI | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | GIH | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | GIH | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01123 | hp1 | a0001 | c0001 | t0007 | g0026 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0269 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0203 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02486 | hp1 | a0001 | c0001 | t0025 | g0126 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0358 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0006 | AFR | MSL | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | USA | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
HG06807 | hp2 | a0001 | c0001 | t0013 | g0366 | AFR | USA | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20300 | hp1 | a0001 | c0001 | t0013 | g0199 | AFR | USA | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0192 | AFR | USA | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0350 | AFR | LWK | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0011 | REF | REF | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0296 | REF | REF | RCL1_chr9_4787944_4866066 | RCL1 | chr9 | 4787944 | 4866066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:4833154 | G | A | 1 | a0002 | 3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
missense_variant&splice_region_variant | MODERATE | c.385G>A | p.Val129Ile | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/9 | 533/2061 | 385/1122 | 129/373 | chr9 | 4833154 | |||
chr9:4834151 | G | T | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.470G>T | p.Arg157Leu | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/9 | 618/2061 | 470/1122 | 157/373 | chr9 | 4834151 | |||
chr9:4834165 | G | A | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.484G>A | p.Gly162Arg | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/9 | 632/2061 | 484/1122 | 162/373 | chr9 | 4834165 | |||
chr9:4841335 | A | G | 1 | a0004 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.688A>G | p.Met230Val | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/9 | 836/2061 | 688/1122 | 230/373 | chr9 | 4841335 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:4793178 | C | A | 1 | a0001c0004 | 2 | HG01099.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.87C>A | p.Pro29Pro | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/9 | 235/2061 | 87/1122 | 29/373 | chr9 | 4793178 | |||
chr9:4834164 | C | T | 1 | a0001c0005 | 2 | HG01192.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.483C>T | p.Pro161Pro | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/9 | 631/2061 | 483/1122 | 161/373 | chr9 | 4834164 | |||
chr9:4834188 | C | T | 1 | a0001c0010 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.507C>T | p.Phe169Phe | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/9 | 655/2061 | 507/1122 | 169/373 | chr9 | 4834188 | |||
chr9:4844549 | G | T | 1 | a0001c0008 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.735G>T | p.Leu245Leu | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/9 | 883/2061 | 735/1122 | 245/373 | chr9 | 4844549 | |||
chr9:4849515 | T | C | 1 | a0001c0007 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.936T>C | p.Val312Val | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/9 | 1084/2061 | 936/1122 | 312/373 | chr9 | 4849515 | |||
chr9:4860182 | C | G | 1 | a0001c0003 | 3 | NA18944.hp1 NA18953.hp2 NA19078.hp2 |
synonymous_variant | LOW | c.1029C>G | p.Thr343Thr | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 1177/2061 | 1029/1122 | 343/373 | chr9 | 4860182 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:4792976 | C | T | 2 | a0001c0001t0035 a0003c0006t0036 |
2 | HG01243.hp2 HG01884.hp2 |
5_prime_UTR_variant | MODIFIER | c.-116C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/9 | 116 | chr9 | 4792976 | ||||||
chr9:4792981 | C | G | 1 | a0001c0001t0034 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/9 | 111 | chr9 | 4792981 | ||||||
chr9:4793033 | C | T | 3 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0033 |
6 | NA18951.hp2 NA18964.hp2 NA18975.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/9 | 59 | chr9 | 4793033 | ||||||
chr9:4860300 | A | G | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(21): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*25A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 25 | chr9 | 4860300 | ||||||
chr9:4860383 | G | C | 1 | a0001c0001t0030 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*108G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 108 | chr9 | 4860383 | ||||||
chr9:4860429 | C | T | 1 | a0001c0001t0009 | 8 | NA18939.hp2 NA18942.hp2 NA18963.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*154C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 154 | chr9 | 4860429 | ||||||
chr9:4860569 | G | A | 31 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(28): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*294G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 294 | chr9 | 4860569 | ||||||
chr9:4860618 | C | T | 4 | a0001c0001t0008 a0001c0001t0014 a0002c0002t0014 others(1): Show |
15 | HG01891.hp2 HG01981.hp1 HG02055.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*343C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 343 | chr9 | 4860618 | ||||||
chr9:4860643 | G | C | 18 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(15): Show |
151 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*368G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 368 | chr9 | 4860643 | ||||||
chr9:4860712 | A | G | 2 | a0001c0001t0008 a0002c0002t0028 |
11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*437A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 437 | chr9 | 4860712 | ||||||
chr9:4860917 | G | GT | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*647dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 648 | INFO_REALIGN_3_PRIME | chr9 | 4860917 | |||||
chr9:4860923 | A | G | 4 | a0001c0001t0014 a0001c0004t0027 a0002c0002t0014 others(1): Show |
6 | HG01981.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*648A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 648 | chr9 | 4860923 | ||||||
chr9:4860943 | A | G | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(13): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*668A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 668 | chr9 | 4860943 | ||||||
chr9:4860964 | T | C | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0007t0003 |
61 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*689T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 689 | chr9 | 4860964 | ||||||
chr9:4860978 | A | G | 1 | a0001c0001t0024 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 703 | chr9 | 4860978 | ||||||
chr9:4860980 | G | A | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(21): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*705G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 705 | chr9 | 4860980 | ||||||
chr9:4861003 | A | T | 1 | a0001c0001t0023 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*728A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 9/9 | 728 | chr9 | 4861003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:4793254 | G | A | 187 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.136+27G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793254 | |||||||
chr9:4793291 | G | C | 8 | a0001c0001t0012g0197 a0001c0001t0013g0192 a0001c0001t0013g0199 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+64G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793291 | |||||||
chr9:4793306 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+79G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793306 | |||||||
chr9:4793394 | G | C | 1 | a0001c0001t0003g0007 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.136+167G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793394 | |||||||
chr9:4793437 | C | T | 2 | a0001c0001t0002g0380 a0001c0001t0010g0379 |
2 | HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.136+210C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793437 | |||||||
chr9:4793528 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+301C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793528 | |||||||
chr9:4793767 | A | C | 1 | a0001c0001t0003g0377 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.136+540A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793767 | |||||||
chr9:4793798 | G | T | 190 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.136+571G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793798 | |||||||
chr9:4793897 | C | A | 8 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(5): Show |
9 | HG00642.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+670C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793897 | |||||||
chr9:4793915 | C | T | 1 | a0001c0001t0004g0373 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.136+688C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793915 | |||||||
chr9:4793944 | G | A | 3 | a0001c0001t0008g0202 a0001c0001t0008g0203 a0001c0001t0030g0201 |
3 | HG02055.hp1 HG02109.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.136+717G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793944 | |||||||
chr9:4793948 | A | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+721A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4793948 | |||||||
chr9:4794163 | C | G | 1 | a0001c0001t0002g0372 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.136+936C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794163 | |||||||
chr9:4794168 | C | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.136+941C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794168 | |||||||
chr9:4794302 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.136+1075G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794302 | |||||||
chr9:4794640 | C | CT | 190 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.136+1427dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4794640 | ||||||
chr9:4794758 | T | C | 79 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(76): Show |
79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.136+1531T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794758 | |||||||
chr9:4794804 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.136+1577A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794804 | |||||||
chr9:4794982 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.136+1755G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794982 | |||||||
chr9:4794991 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0002g0022 |
2 | HG02129.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.136+1764C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4794991 | |||||||
chr9:4795070 | T | C | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.136+1843T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795070 | |||||||
chr9:4795086 | C | CT | 102 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(99): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.136+1868dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4795086 | ||||||
chr9:4795111 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.136+1884T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795111 | |||||||
chr9:4795133 | C | T | 5 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0002g0349 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1906C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795133 | |||||||
chr9:4795180 | C | T | 34 | a0001c0001t0001g0324 a0001c0001t0001g0332 a0001c0001t0001g0333 others(31): Show |
34 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.136+1953C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795180 | |||||||
chr9:4795188 | C | T | 9 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(6): Show |
9 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+1961C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795188 | |||||||
chr9:4795289 | G | A | 9 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(6): Show |
9 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2062G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795289 | |||||||
chr9:4795302 | G | C | 152 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.136+2075G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795302 | |||||||
chr9:4795370 | G | A | 9 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(6): Show |
9 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2143G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795370 | |||||||
chr9:4795490 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0008g0269 others(2): Show |
5 | HG01981.hp1 HG02109.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+2263C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795490 | |||||||
chr9:4795586 | A | G | 2 | a0001c0001t0003g0190 a0001c0001t0035g0277 |
2 | HG00438.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.136+2359A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795586 | |||||||
chr9:4795595 | G | T | 71 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.136+2368G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795595 | |||||||
chr9:4795622 | A | G | 9 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(6): Show |
9 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+2395A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795622 | |||||||
chr9:4795697 | C | T | 1 | a0003c0006t0036g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136+2470C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795697 | |||||||
chr9:4795774 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136+2547C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795774 | |||||||
chr9:4795866 | G | A | 1 | a0001c0001t0006g0315 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.136+2639G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795866 | |||||||
chr9:4795869 | C | T | 2 | a0001c0001t0014g0368 a0001c0005t0004g0378 |
2 | HG01192.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136+2642C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795869 | |||||||
chr9:4795901 | A | T | 1 | a0001c0001t0003g0189 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.136+2674A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795901 | |||||||
chr9:4795917 | G | C | 2 | a0001c0001t0004g0316 a0001c0001t0004g0317 |
2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.136+2690G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795917 | |||||||
chr9:4795924 | G | A | 7 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(4): Show |
8 | HG01099.hp2 HG01891.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+2697G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4795924 | |||||||
chr9:4796032 | A | G | 74 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(71): Show |
74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.136+2805A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796032 | |||||||
chr9:4796110 | C | T | 13 | a0001c0001t0001g0359 a0001c0001t0001g0363 a0001c0001t0001g0364 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.136+2883C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796110 | |||||||
chr9:4796162 | C | T | 105 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(102): Show |
106 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.136+2935C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796162 | |||||||
chr9:4796225 | T | C | 110 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(107): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.136+2998T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796225 | |||||||
chr9:4796258 | A | G | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136+3031A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796258 | |||||||
chr9:4796379 | A | T | 1 | a0001c0001t0002g0188 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.136+3152A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796379 | |||||||
chr9:4796624 | T | G | 74 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(71): Show |
74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.136+3397T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796624 | |||||||
chr9:4796639 | G | A | 1 | a0001c0003t0002g0019 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.136+3412G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796639 | |||||||
chr9:4796820 | G | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0302 a0001c0001t0002g0303 others(2): Show |
6 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3593G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796820 | |||||||
chr9:4796822 | G | GT | 5 | a0001c0001t0002g0005 a0001c0001t0002g0302 a0001c0001t0002g0303 others(2): Show |
6 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3595_136+3596i others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796822 | |||||||
chr9:4796823 | C | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0302 a0001c0001t0002g0303 others(2): Show |
6 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3596C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796823 | |||||||
chr9:4796841 | T | C | 6 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 others(3): Show |
6 | HG00642.hp1 HG01106.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3614T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796841 | |||||||
chr9:4796943 | A | G | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0369 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+3716A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4796943 | |||||||
chr9:4797830 | C | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+4603C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4797830 | |||||||
chr9:4797900 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.136+4673G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4797900 | |||||||
chr9:4797960 | ATTAAGT | A | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0369 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+4737_136+4742d others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4797960 | ||||||
chr9:4798056 | G | A | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+4829G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798056 | |||||||
chr9:4798087 | C | A | 35 | a0001c0001t0001g0324 a0001c0001t0001g0332 a0001c0001t0001g0333 others(32): Show |
35 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.136+4860C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798087 | |||||||
chr9:4798112 | A | G | 2 | a0001c0001t0014g0194 a0001c0001t0014g0195 |
2 | HG01981.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.136+4885A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798112 | |||||||
chr9:4798148 | C | G | 2 | a0001c0001t0008g0202 a0001c0001t0008g0203 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.136+4921C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798148 | |||||||
chr9:4798150 | C | G | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+4923C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798150 | |||||||
chr9:4798211 | A | G | 1 | a0001c0001t0032g0187 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+4984A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798211 | |||||||
chr9:4798261 | G | C | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+5034G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798261 | |||||||
chr9:4798362 | C | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+5135C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798362 | |||||||
chr9:4798368 | C | T | 46 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(43): Show |
46 | HG00741.hp2 HG01074.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+5141C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798368 | |||||||
chr9:4798465 | C | A | 12 | a0001c0001t0001g0359 a0001c0001t0001g0363 a0001c0001t0001g0364 others(9): Show |
12 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.136+5238C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798465 | |||||||
chr9:4798508 | G | A | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136+5281G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798508 | |||||||
chr9:4798509 | A | G | 2 | a0001c0001t0014g0194 a0001c0001t0014g0195 |
2 | HG01981.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.136+5282A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798509 | |||||||
chr9:4798878 | CT | C | 336 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0024 others(333): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.136+5670delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4798878 | ||||||
chr9:4798878 | CTT | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0029 others(26): Show |
29 | HG00741.hp2 HG01123.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.136+5669_136+5670d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4798878 | ||||||
chr9:4798882 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0005g0279 a0001c0001t0005g0280 |
3 | HG00597.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.136+5655T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4798882 | |||||||
chr9:4798974 | CCTTTT | C | 4 | a0001c0001t0001g0359 a0001c0001t0002g0321 a0001c0001t0008g0360 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+5764_136+5768d others(7): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4798974 | ||||||
chr9:4799047 | C | G | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+5820C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799047 | |||||||
chr9:4799071 | C | T | 1 | a0001c0001t0012g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136+5844C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799071 | |||||||
chr9:4799084 | T | C | 54 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(51): Show |
54 | HG00741.hp2 HG01074.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.136+5857T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799084 | |||||||
chr9:4799116 | C | CCCTT | 144 | a0001c0001t0001g0037 a0001c0001t0001g0214 a0001c0001t0001g0217 others(141): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.136+5892_136+5893i others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4799116 | ||||||
chr9:4799122 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+5895C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799122 | |||||||
chr9:4799262 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.136+6035C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799262 | |||||||
chr9:4799274 | G | A | 1 | a0001c0001t0006g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.136+6047G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799274 | |||||||
chr9:4799305 | A | G | 1 | a0001c0001t0002g0343 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+6078A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799305 | |||||||
chr9:4799564 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.136+6337T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799564 | |||||||
chr9:4799577 | G | C | 64 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0092 others(61): Show |
64 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.136+6350G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799577 | |||||||
chr9:4799601 | T | C | 6 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0369 others(3): Show |
6 | HG02615.hp1 HG02630.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+6374T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799601 | |||||||
chr9:4799718 | A | T | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.136+6491A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799718 | |||||||
chr9:4799781 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0002g0264 |
2 | NA18978.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.136+6554C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799781 | |||||||
chr9:4799869 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+6642G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799869 | |||||||
chr9:4799875 | C | T | 2 | a0001c0001t0014g0368 a0001c0010t0001g0272 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.136+6648C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799875 | |||||||
chr9:4799960 | A | G | 5 | a0001c0001t0014g0368 a0001c0001t0035g0277 a0001c0008t0026g0200 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+6733A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4799960 | |||||||
chr9:4800169 | A | G | 2 | a0001c0001t0010g0179 a0001c0001t0010g0180 |
2 | NA18983.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.136+6942A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800169 | |||||||
chr9:4800173 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.136+6946C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800173 | |||||||
chr9:4800217 | T | A | 1 | a0001c0001t0002g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+6990T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800217 | |||||||
chr9:4800335 | T | G | 1 | a0001c0001t0002g0372 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.136+7108T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800335 | |||||||
chr9:4800403 | C | T | 4 | a0001c0001t0014g0194 a0001c0001t0014g0195 a0002c0002t0004g0198 others(1): Show |
4 | HG01981.hp1 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+7176C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800403 | |||||||
chr9:4800430 | G | T | 36 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(33): Show |
36 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.136+7203G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800430 | |||||||
chr9:4800445 | T | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+7218T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800445 | |||||||
chr9:4800492 | G | C | 1 | a0001c0001t0003g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.136+7265G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800492 | |||||||
chr9:4800517 | G | T | 2 | a0001c0001t0014g0368 a0001c0010t0001g0272 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.136+7290G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800517 | |||||||
chr9:4800588 | G | A | 1 | a0005c0011t0031g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+7361G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800588 | |||||||
chr9:4800599 | G | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+7372G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800599 | |||||||
chr9:4800652 | A | AT | 91 | a0001c0001t0001g0176 a0001c0001t0001g0214 a0001c0001t0001g0217 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.136+7443dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4800652 | ||||||
chr9:4800652 | A | ATT | 9 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(6): Show |
9 | HG01192.hp1 HG02055.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+7442_136+7443d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4800652 | ||||||
chr9:4800652 | AT | A | 11 | a0001c0001t0001g0097 a0001c0001t0001g0355 a0001c0001t0005g0353 others(8): Show |
12 | HG01099.hp2 HG01891.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+7443delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4800652 | ||||||
chr9:4800652 | ATTT | A | 36 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(33): Show |
36 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.136+7441_136+7443d others(5): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4800652 | ||||||
chr9:4800780 | G | A | 1 | a0001c0001t0008g0352 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.136+7553G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800780 | |||||||
chr9:4800843 | G | A | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.136+7616G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800843 | |||||||
chr9:4800895 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.136+7668C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800895 | |||||||
chr9:4800932 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0008g0202 a0001c0001t0008g0203 |
3 | HG02055.hp1 HG02109.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.136+7705G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800932 | |||||||
chr9:4800948 | T | C | 79 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(76): Show |
79 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.136+7721T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800948 | |||||||
chr9:4800960 | A | G | 2 | a0001c0001t0008g0360 a0001c0001t0008g0361 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+7733A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800960 | |||||||
chr9:4800982 | A | C | 7 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(4): Show |
8 | HG01099.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+7755A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4800982 | |||||||
chr9:4801052 | G | A | 11 | a0001c0001t0001g0042 a0001c0001t0007g0040 a0001c0001t0007g0043 others(8): Show |
11 | HG01081.hp2 HG01433.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+7825G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801052 | |||||||
chr9:4801088 | G | A | 40 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(37): Show |
40 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.136+7861G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801088 | |||||||
chr9:4801147 | T | C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(33): Show |
36 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.136+7920T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801147 | |||||||
chr9:4801159 | G | A | 1 | a0005c0011t0031g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.136+7932G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801159 | |||||||
chr9:4801264 | TGGGCGTA others(3): Show |
T | 1 | a0001c0001t0001g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.136+8038_136+8047d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801264 | |||||||
chr9:4801296 | C | T | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(9): Show |
12 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+8069C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801296 | |||||||
chr9:4801305 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136+8078G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801305 | |||||||
chr9:4801323 | C | A | 6 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(3): Show |
6 | HG02145.hp2 HG03130.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+8096C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801323 | |||||||
chr9:4801366 | C | T | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.136+8139C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801366 | |||||||
chr9:4801369 | G | A | 1 | a0001c0001t0022g0051 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.136+8142G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801369 | |||||||
chr9:4801469 | G | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+8242G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801469 | |||||||
chr9:4801502 | C | G | 15 | a0001c0001t0001g0311 a0001c0001t0001g0313 a0001c0001t0001g0359 others(12): Show |
15 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+8275C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801502 | |||||||
chr9:4801563 | C | T | 18 | a0001c0001t0001g0311 a0001c0001t0001g0313 a0001c0001t0001g0359 others(15): Show |
18 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.136+8336C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801563 | |||||||
chr9:4801645 | T | C | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+8418T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801645 | |||||||
chr9:4801668 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG02896.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+8441A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801668 | |||||||
chr9:4801708 | G | C | 11 | a0001c0001t0001g0042 a0001c0001t0007g0040 a0001c0001t0007g0043 others(8): Show |
11 | HG01081.hp2 HG01433.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+8481G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801708 | |||||||
chr9:4801718 | C | CT | 8 | a0001c0001t0001g0172 a0001c0001t0001g0376 a0001c0001t0013g0199 others(5): Show |
8 | HG02922.hp2 HG03669.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+8509dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4801718 | ||||||
chr9:4801718 | CT | C | 49 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0311 others(46): Show |
49 | HG01074.hp2 HG01192.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.136+8509delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4801718 | ||||||
chr9:4801718 | CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(9): Show |
12 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+8499_136+8509d others(13): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4801718 | ||||||
chr9:4801783 | C | G | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+8556C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801783 | |||||||
chr9:4801809 | C | G | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+8582C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801809 | |||||||
chr9:4801840 | G | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+8613G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801840 | |||||||
chr9:4801901 | C | T | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+8674C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801901 | |||||||
chr9:4801920 | C | CT | 9 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(6): Show |
10 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+8702dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4801920 | ||||||
chr9:4801934 | C | A | 2 | a0002c0002t0004g0198 a0002c0002t0028g0018 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136+8707C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801934 | |||||||
chr9:4801942 | C | T | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+8715C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801942 | |||||||
chr9:4801964 | G | A | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+8737G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801964 | |||||||
chr9:4801973 | A | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0009g0003 others(3): Show |
7 | NA18939.hp2 NA18942.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+8746A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4801973 | |||||||
chr9:4802032 | C | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG01993.hp2 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+8805C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802032 | |||||||
chr9:4802074 | A | AT | 7 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0001g0266 others(4): Show |
7 | HG01978.hp2 HG02148.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+8870dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4802074 | ||||||
chr9:4802074 | AT | A | 213 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(210): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.136+8870delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4802074 | ||||||
chr9:4802074 | ATT | A | 9 | a0001c0001t0001g0029 a0001c0001t0001g0355 a0001c0001t0003g0190 others(6): Show |
10 | HG00438.hp2 HG01099.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.136+8869_136+8870d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4802074 | ||||||
chr9:4802074 | ATTT | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+8868_136+8870d others(5): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4802074 | ||||||
chr9:4802087 | T | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+8860T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802087 | |||||||
chr9:4802113 | C | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+8886C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802113 | |||||||
chr9:4802145 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.136+8918G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802145 | |||||||
chr9:4802172 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG02896.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+8945G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802172 | |||||||
chr9:4802228 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.136+9001A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802228 | |||||||
chr9:4802262 | C | A | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+9035C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802262 | |||||||
chr9:4802316 | C | G | 2 | a0001c0001t0014g0368 a0001c0010t0001g0272 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.136+9089C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802316 | |||||||
chr9:4802357 | T | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+9130T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802357 | |||||||
chr9:4802388 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.136+9161C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802388 | |||||||
chr9:4802448 | G | A | 15 | a0001c0001t0001g0311 a0001c0001t0001g0313 a0001c0001t0001g0359 others(12): Show |
15 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+9221G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802448 | |||||||
chr9:4802483 | G | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+9256G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802483 | |||||||
chr9:4802536 | T | C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(33): Show |
36 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.136+9309T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802536 | |||||||
chr9:4802564 | C | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+9337C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802564 | |||||||
chr9:4802626 | AT | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+9408delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4802626 | ||||||
chr9:4802657 | C | G | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | NA18947.hp2 NA18954.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+9430C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802657 | |||||||
chr9:4802821 | G | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+9594G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802821 | |||||||
chr9:4802859 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.136+9632C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802859 | |||||||
chr9:4802884 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0009g0104 |
3 | NA18952.hp2 NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.136+9657G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802884 | |||||||
chr9:4802939 | G | C | 31 | a0001c0001t0001g0037 a0001c0001t0001g0332 a0001c0001t0001g0333 others(28): Show |
31 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.136+9712G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4802939 | |||||||
chr9:4803015 | C | CT | 8 | a0001c0001t0001g0266 a0001c0001t0001g0355 a0001c0001t0003g0007 others(5): Show |
9 | HG01099.hp2 HG01258.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+9801dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4803015 | ||||||
chr9:4803065 | A | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0324 a0001c0001t0001g0332 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+9838A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803065 | |||||||
chr9:4803105 | C | T | 2 | a0001c0001t0002g0095 a0001c0001t0004g0158 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136+9878C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803105 | |||||||
chr9:4803112 | G | C | 2 | a0001c0001t0020g0052 a0001c0001t0020g0053 |
2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.136+9885G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803112 | |||||||
chr9:4803284 | A | T | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.136+10057A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803284 | |||||||
chr9:4803328 | T | A | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+10101T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803328 | |||||||
chr9:4803436 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.136+10209G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803436 | |||||||
chr9:4803475 | G | T | 2 | a0001c0001t0035g0277 a0003c0006t0036g0196 |
2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.136+10248G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803475 | |||||||
chr9:4803510 | T | C | 1 | a0001c0001t0001g0217 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.136+10283T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803510 | |||||||
chr9:4803573 | A | G | 1 | a0001c0001t0002g0267 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.136+10346A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803573 | |||||||
chr9:4803649 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136+10422C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803649 | |||||||
chr9:4803651 | G | C | 149 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.136+10424G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803651 | |||||||
chr9:4803666 | C | T | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(9): Show |
12 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.136+10439C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803666 | |||||||
chr9:4803677 | G | C | 1 | a0001c0001t0003g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.136+10450G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803677 | |||||||
chr9:4803715 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.136+10488A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803715 | |||||||
chr9:4803725 | G | T | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | NA18947.hp2 NA18954.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+10498G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803725 | |||||||
chr9:4803726 | TA | T | 17 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(14): Show |
17 | HG01192.hp1 HG01981.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.136+10511delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4803726 | ||||||
chr9:4803844 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.136+10617A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803844 | |||||||
chr9:4803863 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.136+10636G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803863 | |||||||
chr9:4803871 | C | G | 1 | a0001c0001t0034g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.136+10644C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803871 | |||||||
chr9:4803973 | G | C | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+10746G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4803973 | |||||||
chr9:4804022 | A | T | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+10795A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804022 | |||||||
chr9:4804140 | G | T | 1 | a0003c0006t0036g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136+10913G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804140 | |||||||
chr9:4804215 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+10988G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804215 | |||||||
chr9:4804224 | T | A | 1 | a0001c0001t0003g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.136+10997T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804224 | |||||||
chr9:4804273 | G | A | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.136+11046G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804273 | |||||||
chr9:4804342 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0004g0158 |
2 | HG01884.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.136+11115G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804342 | |||||||
chr9:4804389 | G | A | 85 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(82): Show |
86 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.136+11162G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804389 | |||||||
chr9:4804411 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.136+11184C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804411 | |||||||
chr9:4804430 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136+11203C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804430 | |||||||
chr9:4804449 | A | G | 141 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(138): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.136+11222A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804449 | |||||||
chr9:4804453 | C | G | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+11226C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804453 | |||||||
chr9:4804474 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.136+11247C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804474 | |||||||
chr9:4804564 | C | T | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.136+11337C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804564 | |||||||
chr9:4804601 | C | A | 10 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(7): Show |
11 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+11374C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804601 | |||||||
chr9:4804632 | C | T | 2 | a0001c0001t0008g0360 a0001c0001t0008g0361 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.136+11405C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804632 | |||||||
chr9:4804703 | C | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+11476C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804703 | |||||||
chr9:4804745 | A | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+11518A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804745 | |||||||
chr9:4804772 | G | A | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+11545G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804772 | |||||||
chr9:4804805 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0005g0278 |
3 | HG03209.hp1 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.136+11578C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804805 | |||||||
chr9:4804901 | A | G | 148 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(145): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.136+11674A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804901 | |||||||
chr9:4804915 | G | A | 2 | a0001c0001t0003g0326 a0001c0001t0015g0325 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136+11688G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4804915 | |||||||
chr9:4805019 | G | A | 1 | a0001c0001t0001g0376 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.136+11792G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805019 | |||||||
chr9:4805127 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.136+11900G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805127 | |||||||
chr9:4805188 | A | G | 15 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(12): Show |
15 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.136+11961A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805188 | |||||||
chr9:4805208 | TAAGCA | T | 5 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(2): Show |
5 | HG02145.hp2 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+11984_136+1198 others(9): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805208 | ||||||
chr9:4805222 | A | C | 148 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(145): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.136+11995A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805222 | |||||||
chr9:4805243 | T | C | 11 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(8): Show |
12 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.136+12016T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805243 | |||||||
chr9:4805389 | G | A | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+12162G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805389 | |||||||
chr9:4805396 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.136+12169A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805396 | |||||||
chr9:4805400 | A | AGAAGGG | 214 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(211): Show |
218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.136+12191_136+1219 others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805400 | ||||||
chr9:4805400 | A | AGAAGGGG others(5): Show |
1 | a0001c0001t0030g0201 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.136+12185_136+1219 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805400 | ||||||
chr9:4805449 | C | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG00423.hp2 NA18747.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+12222C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805449 | |||||||
chr9:4805452 | AGATCCTT others(5): Show |
A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+12242_136+1225 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805452 | ||||||
chr9:4805468 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.136+12241C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805468 | |||||||
chr9:4805503 | TA | T | 4 | a0001c0001t0001g0300 a0001c0001t0002g0298 a0001c0001t0002g0299 others(1): Show |
4 | HG02257.hp1 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+12284delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805503 | ||||||
chr9:4805541 | A | G | 1 | a0001c0001t0002g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.136+12314A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805541 | |||||||
chr9:4805550 | T | C | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+12323T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805550 | |||||||
chr9:4805592 | C | G | 147 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.136+12365C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805592 | |||||||
chr9:4805679 | G | A | 1 | a0001c0001t0003g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.136+12452G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805679 | |||||||
chr9:4805680 | G | A | 1 | a0001c0001t0003g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.136+12453G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805680 | |||||||
chr9:4805712 | A | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.136+12485A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805712 | |||||||
chr9:4805760 | T | G | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.136+12533T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805760 | |||||||
chr9:4805824 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.136+12597C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805824 | |||||||
chr9:4805844 | CAG | C | 8 | a0001c0001t0003g0088 a0001c0001t0006g0082 a0001c0001t0006g0083 others(5): Show |
8 | NA18951.hp1 NA18962.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+12620_136+1262 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4805844 | ||||||
chr9:4805962 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136+12735C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4805962 | |||||||
chr9:4806012 | A | G | 2 | a0001c0001t0003g0080 a0001c0001t0005g0081 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.136+12785A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806012 | |||||||
chr9:4806017 | G | GGT | 68 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0092 others(65): Show |
68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.136+12817_136+1281 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806017 | ||||||
chr9:4806017 | GGT | G | 99 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(96): Show |
101 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.136+12817_136+1281 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806017 | ||||||
chr9:4806017 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.136+12809_136+1281 others(14): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806017 | ||||||
chr9:4806019 | T | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0295 |
2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.136+12792T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806019 | |||||||
chr9:4806030 | G | GTGTGTGT others(5): Show |
3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG00140.hp2 HG00280.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.136+12814_136+1281 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806030 | ||||||
chr9:4806036 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0004g0317 a0001c0001t0006g0319 |
2 | HG01496.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.136+12818_136+1281 others(22): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806036 | ||||||
chr9:4806036 | G | GTGTGTGT others(9): Show |
7 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0002g0339 others(4): Show |
7 | HG01993.hp1 NA18939.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(20): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806036 | ||||||
chr9:4806036 | G | GTGTGTGT others(7): Show |
6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(18): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806036 | ||||||
chr9:4806038 | G | GTGTGTGT others(11): Show |
3 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0343 |
3 | HG02145.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.136+12818_136+1281 others(22): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806038 | ||||||
chr9:4806038 | G | GTGTGTGT others(9): Show |
10 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0356 others(7): Show |
10 | HG01074.hp2 HG02486.hp2 HG03579.hp2 others(7): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(20): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806038 | ||||||
chr9:4806038 | G | GTGTGTGT others(7): Show |
8 | a0001c0001t0001g0106 a0001c0001t0001g0332 a0001c0001t0001g0333 others(5): Show |
8 | HG02698.hp2 HG03688.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(18): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806038 | ||||||
chr9:4806038 | G | GTGTGTGT others(5): Show |
2 | a0001c0001t0001g0037 a0001c0001t0004g0341 |
2 | HG03927.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.136+12818_136+1281 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806038 | ||||||
chr9:4806040 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0002g0219 a0001c0001t0004g0370 |
2 | HG00140.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.136+12818_136+1281 others(18): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806040 | ||||||
chr9:4806040 | G | GTGTGTGT others(3): Show |
8 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0247 others(5): Show |
8 | HG01069.hp1 HG01515.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(14): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806040 | ||||||
chr9:4806042 | G | GTGTGTGT others(5): Show |
1 | a0003c0006t0036g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.136+12818_136+1281 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806042 | ||||||
chr9:4806042 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0259 |
2 | HG04204.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.136+12818_136+1281 others(14): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806042 | ||||||
chr9:4806042 | G | GTGTGTGT others(1): Show |
71 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(68): Show |
71 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806042 | ||||||
chr9:4806042 | G | GTGTGTT | 3 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0251 |
4 | HG00642.hp2 HG03239.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806042 | ||||||
chr9:4806042 | G | T | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+12815G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806042 | |||||||
chr9:4806044 | G | GTGTGTGT others(1): Show |
4 | a0001c0001t0003g0326 a0001c0001t0012g0197 a0001c0001t0012g0344 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+12818_136+1281 others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806044 | ||||||
chr9:4806044 | G | T | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.136+12817G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806044 | |||||||
chr9:4806046 | T | G | 147 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.136+12819T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806046 | |||||||
chr9:4806046 | T | TTGTG | 3 | a0001c0001t0014g0195 a0002c0002t0004g0198 a0002c0002t0028g0018 |
3 | HG02572.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.136+12833_136+1283 others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806046 | ||||||
chr9:4806046 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0004g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.136+12827_136+1283 others(14): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806046 | ||||||
chr9:4806064 | T | G | 156 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(153): Show |
158 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.136+12837T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806064 | |||||||
chr9:4806118 | G | GT | 10 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(7): Show |
11 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.136+12900dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806118 | ||||||
chr9:4806127 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.136+12900T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806127 | |||||||
chr9:4806146 | A | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.136+12919A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806146 | |||||||
chr9:4806233 | T | C | 99 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(96): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.136+13006T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806233 | |||||||
chr9:4806247 | A | C | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.136+13020A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806247 | |||||||
chr9:4806520 | G | A | 86 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(83): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.136+13293G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806520 | |||||||
chr9:4806556 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.136+13329C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806556 | |||||||
chr9:4806580 | C | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+13353C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806580 | |||||||
chr9:4806587 | T | TAC | 22 | a0001c0001t0001g0146 a0001c0001t0001g0295 a0001c0001t0001g0307 others(19): Show |
22 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.136+13406_136+1340 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | T | TACAC | 5 | a0001c0001t0001g0273 a0001c0001t0001g0306 a0001c0001t0003g0108 others(2): Show |
5 | HG01361.hp1 HG01934.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+13404_136+1340 others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | T | TACACAC | 5 | a0001c0001t0001g0346 a0001c0001t0003g0054 a0001c0001t0003g0189 others(2): Show |
5 | HG00735.hp1 HG02015.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+13402_136+1340 others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TAC | T | 51 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0099 others(48): Show |
52 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.136+13406_136+1340 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACAC | T | 160 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0028 others(157): Show |
161 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.136+13404_136+1340 others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACAC | T | 23 | a0001c0001t0001g0105 a0001c0001t0001g0270 a0001c0001t0001g0271 others(20): Show |
24 | HG00597.hp1 HG00642.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.136+13402_136+1340 others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(1): Show |
T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG02896.hp2 HG02965.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.136+13400_136+1340 others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(3): Show |
T | 7 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(4): Show |
8 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+13398_136+1340 others(14): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(5): Show |
T | 4 | a0001c0001t0002g0305 a0001c0001t0003g0326 a0001c0001t0012g0197 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+13396_136+1340 others(16): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.136+13392_136+1340 others(20): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(11): Show |
T | 8 | a0001c0001t0001g0154 a0001c0001t0001g0168 a0001c0001t0009g0003 others(5): Show |
9 | HG02015.hp1 NA18939.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+13390_136+1340 others(22): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(13): Show |
T | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.136+13388_136+1340 others(24): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806587 | TACACACA others(17): Show |
T | 1 | a0001c0001t0001g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+13384_136+1340 others(28): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806587 | ||||||
chr9:4806633 | C | CACACAT | 4 | a0001c0001t0001g0363 a0001c0001t0001g0364 a0001c0001t0001g0365 others(1): Show |
4 | HG02559.hp1 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+13407_136+1340 others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806633 | ||||||
chr9:4806633 | C | CAT | 5 | a0001c0001t0001g0359 a0001c0001t0002g0321 a0001c0001t0002g0322 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+13410_136+1341 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806633 | ||||||
chr9:4806633 | C | T | 57 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(54): Show |
58 | HG00741.hp1 HG01074.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.136+13406C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806633 | |||||||
chr9:4806702 | C | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.136+13475C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806702 | |||||||
chr9:4806723 | G | GT | 43 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0306 others(40): Show |
43 | HG00741.hp2 HG01074.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.136+13506dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4806723 | ||||||
chr9:4806795 | A | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.136+13568A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4806795 | |||||||
chr9:4807130 | G | A | 2 | a0001c0001t0002g0219 a0001c0001t0002g0247 |
2 | HG00140.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.136+13903G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807130 | |||||||
chr9:4807270 | G | T | 1 | a0001c0001t0002g0372 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.136+14043G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807270 | |||||||
chr9:4807380 | T | C | 47 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(44): Show |
48 | HG01074.hp2 HG01099.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.136+14153T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807380 | |||||||
chr9:4807439 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.136+14212G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807439 | |||||||
chr9:4807553 | C | G | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136+14326C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807553 | |||||||
chr9:4807570 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.136+14343A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807570 | |||||||
chr9:4807588 | C | T | 1 | a0001c0001t0006g0319 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.136+14361C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807588 | |||||||
chr9:4807612 | C | T | 2 | a0001c0001t0003g0326 a0001c0001t0015g0325 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.136+14385C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807612 | |||||||
chr9:4807673 | A | C | 368 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(365): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.136+14446A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807673 | |||||||
chr9:4807770 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136+14543G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807770 | |||||||
chr9:4807790 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.136+14563A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807790 | |||||||
chr9:4807806 | C | A | 149 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.136+14579C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807806 | |||||||
chr9:4807875 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136+14648C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807875 | |||||||
chr9:4807901 | C | T | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.136+14674C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4807901 | |||||||
chr9:4808069 | C | T | 149 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.136+14842C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808069 | |||||||
chr9:4808186 | A | G | 2 | a0001c0001t0012g0197 a0001c0001t0012g0344 |
2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.136+14959A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808186 | |||||||
chr9:4808305 | T | A | 3 | a0001c0001t0001g0359 a0001c0001t0008g0202 a0001c0001t0008g0203 |
3 | HG02055.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.136+15078T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808305 | |||||||
chr9:4808363 | A | G | 3 | a0001c0001t0013g0199 a0001c0001t0013g0366 a0001c0004t0027g0193 |
3 | HG02922.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.136+15136A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808363 | |||||||
chr9:4808377 | G | A | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136+15150G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808377 | |||||||
chr9:4808430 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.137-15118C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808430 | |||||||
chr9:4808456 | C | T | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.137-15092C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808456 | |||||||
chr9:4808506 | C | T | 2 | a0001c0001t0013g0192 a0001c0004t0027g0193 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-15042C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808506 | |||||||
chr9:4808527 | C | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-15021C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808527 | |||||||
chr9:4808531 | T | A | 149 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.137-15017T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808531 | |||||||
chr9:4808721 | G | A | 1 | a0001c0001t0005g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.137-14827G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808721 | |||||||
chr9:4808735 | A | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-14813A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808735 | |||||||
chr9:4808794 | G | A | 149 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(146): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.137-14754G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808794 | |||||||
chr9:4808799 | C | T | 147 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(144): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.137-14749C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808799 | |||||||
chr9:4808830 | G | A | 150 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(147): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.137-14718G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808830 | |||||||
chr9:4808857 | T | C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(12): Show |
16 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-14691T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808857 | |||||||
chr9:4808906 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.137-14642C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808906 | |||||||
chr9:4808908 | A | C | 1 | a0001c0001t0004g0118 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.137-14640A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808908 | |||||||
chr9:4808971 | C | T | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-14577C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4808971 | |||||||
chr9:4809126 | G | T | 1 | a0001c0001t0002g0212 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.137-14422G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809126 | |||||||
chr9:4809158 | T | G | 65 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0092 others(62): Show |
65 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.137-14390T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809158 | |||||||
chr9:4809220 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-14328C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809220 | |||||||
chr9:4809244 | C | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02896.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-14304C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809244 | |||||||
chr9:4809391 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.137-14157C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809391 | |||||||
chr9:4809423 | C | T | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137-14125C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809423 | |||||||
chr9:4809471 | G | A | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.137-14077G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809471 | |||||||
chr9:4809551 | G | A | 8 | a0001c0001t0003g0025 a0001c0001t0003g0061 a0001c0001t0003g0062 others(5): Show |
8 | HG00621.hp1 HG02015.hp2 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-13997G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809551 | |||||||
chr9:4809588 | G | A | 40 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(37): Show |
40 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.137-13960G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809588 | |||||||
chr9:4809597 | T | C | 3 | a0001c0001t0001g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 |
3 | HG02055.hp2 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-13951T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809597 | |||||||
chr9:4809600 | A | G | 3 | a0001c0001t0001g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 |
3 | HG02055.hp2 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-13948A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809600 | |||||||
chr9:4809604 | G | A | 135 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(132): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.137-13944G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809604 | |||||||
chr9:4809655 | C | T | 2 | a0001c0001t0014g0194 a0001c0001t0014g0195 |
2 | HG01981.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.137-13893C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809655 | |||||||
chr9:4809784 | C | T | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137-13764C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809784 | |||||||
chr9:4809919 | C | T | 2 | a0001c0001t0014g0368 a0001c0010t0001g0272 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.137-13629C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809919 | |||||||
chr9:4809989 | G | A | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-13559G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809989 | |||||||
chr9:4809991 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG02896.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-13557A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4809991 | |||||||
chr9:4810017 | A | G | 87 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(84): Show |
88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.137-13531A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810017 | |||||||
chr9:4810023 | G | T | 1 | a0001c0001t0004g0316 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.137-13525G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810023 | |||||||
chr9:4810029 | C | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-13519C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810029 | |||||||
chr9:4810037 | G | A | 1 | a0003c0006t0036g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137-13511G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810037 | |||||||
chr9:4810084 | T | C | 3 | a0001c0001t0002g0076 a0001c0001t0003g0075 a0001c0001t0003g0093 |
3 | HG00099.hp1 HG01175.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.137-13464T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810084 | |||||||
chr9:4810094 | C | G | 1 | a0001c0003t0002g0019 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.137-13454C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810094 | |||||||
chr9:4810097 | A | G | 138 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.137-13451A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810097 | |||||||
chr9:4810117 | C | T | 14 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(11): Show |
15 | HG01099.hp2 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-13431C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810117 | |||||||
chr9:4810196 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-13352C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810196 | |||||||
chr9:4810202 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-13346G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810202 | |||||||
chr9:4810251 | A | T | 2 | a0001c0001t0002g0281 a0001c0001t0002g0283 |
2 | HG01123.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.137-13297A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810251 | |||||||
chr9:4810363 | G | A | 1 | a0001c0001t0019g0027 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.137-13185G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810363 | |||||||
chr9:4810373 | T | G | 3 | a0001c0001t0004g0166 a0001c0001t0004g0316 a0001c0001t0004g0317 |
3 | HG01496.hp1 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.137-13175T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810373 | |||||||
chr9:4810453 | G | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-13095G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810453 | |||||||
chr9:4810529 | C | T | 2 | a0001c0001t0012g0357 a0001c0001t0012g0358 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.137-13019C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810529 | |||||||
chr9:4810539 | TTC | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.137-13007_137-1300 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4810539 | ||||||
chr9:4810645 | T | TG | 154 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0214 others(151): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.137-12902dupG | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4810645 | ||||||
chr9:4810686 | C | T | 1 | a0005c0011t0031g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.137-12862C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810686 | |||||||
chr9:4810687 | G | A | 1 | a0001c0001t0006g0327 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.137-12861G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810687 | |||||||
chr9:4810844 | T | C | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.137-12704T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810844 | |||||||
chr9:4810910 | A | G | 2 | a0001c0001t0002g0001 a0001c0001t0002g0012 |
3 | HG00642.hp2 HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.137-12638A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4810910 | |||||||
chr9:4810972 | G | GTA | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-12573_137-1257 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4810972 | ||||||
chr9:4811083 | A | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-12465A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811083 | |||||||
chr9:4811148 | G | A | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.137-12400G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811148 | |||||||
chr9:4811197 | A | T | 6 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(3): Show |
6 | HG02145.hp2 HG03130.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-12351A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811197 | |||||||
chr9:4811226 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0002g0110 |
2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.137-12322G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811226 | |||||||
chr9:4811279 | C | CA | 7 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 others(4): Show |
7 | HG00642.hp1 HG01106.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-12255dupA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4811279 | ||||||
chr9:4811291 | A | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-12257A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811291 | |||||||
chr9:4811315 | A | G | 4 | a0001c0001t0003g0326 a0001c0001t0012g0197 a0001c0001t0012g0344 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.137-12233A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811315 | |||||||
chr9:4811442 | G | A | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.137-12106G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811442 | |||||||
chr9:4811553 | A | C | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-11995A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811553 | |||||||
chr9:4811553 | A | G | 99 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
101 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.137-11995A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811553 | |||||||
chr9:4811568 | C | G | 1 | a0001c0001t0001g0371 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.137-11980C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811568 | |||||||
chr9:4811691 | G | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-11857G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811691 | |||||||
chr9:4811701 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0178 |
2 | HG00735.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.137-11847C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811701 | |||||||
chr9:4811869 | T | C | 2 | a0001c0001t0003g0077 a0001c0001t0003g0078 |
2 | HG02723.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.137-11679T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811869 | |||||||
chr9:4811896 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.137-11652T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4811896 | |||||||
chr9:4812068 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.137-11480G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812068 | |||||||
chr9:4812116 | T | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-11432T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812116 | |||||||
chr9:4812149 | G | C | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-11399G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812149 | |||||||
chr9:4812288 | A | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-11260A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812288 | |||||||
chr9:4812303 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.137-11245A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812303 | |||||||
chr9:4812344 | AT | A | 169 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(166): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.137-11193delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4812344 | ||||||
chr9:4812344 | ATT | A | 87 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0226 others(84): Show |
88 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.137-11194_137-1119 others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4812344 | ||||||
chr9:4812452 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-11096C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812452 | |||||||
chr9:4812498 | A | G | 1 | a0001c0001t0005g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137-11050A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812498 | |||||||
chr9:4812550 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-10998G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812550 | |||||||
chr9:4812610 | T | C | 1 | a0001c0001t0016g0225 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137-10938T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812610 | |||||||
chr9:4812679 | C | G | 91 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0231 others(88): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-10869C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812679 | |||||||
chr9:4812693 | G | C | 2 | a0001c0001t0011g0244 a0001c0001t0011g0245 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.137-10855G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812693 | |||||||
chr9:4812746 | T | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-10802T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812746 | |||||||
chr9:4812912 | A | G | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-10636A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812912 | |||||||
chr9:4812968 | C | T | 2 | a0001c0001t0013g0192 a0001c0004t0027g0193 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-10580C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4812968 | |||||||
chr9:4813090 | A | C | 92 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(89): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.137-10458A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813090 | |||||||
chr9:4813146 | G | C | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-10402G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813146 | |||||||
chr9:4813222 | A | G | 4 | a0001c0001t0014g0368 a0001c0001t0035g0277 a0001c0010t0001g0272 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-10326A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813222 | |||||||
chr9:4813233 | A | T | 2 | a0001c0001t0013g0192 a0001c0004t0027g0193 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-10315A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813233 | |||||||
chr9:4813261 | G | C | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-10287G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813261 | |||||||
chr9:4813268 | A | C | 1 | a0001c0001t0006g0327 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.137-10280A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813268 | |||||||
chr9:4813337 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.137-10211C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813337 | |||||||
chr9:4813339 | A | G | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.137-10209A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813339 | |||||||
chr9:4813386 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-10162C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813386 | |||||||
chr9:4813406 | A | G | 1 | a0001c0001t0003g0345 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137-10142A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813406 | |||||||
chr9:4813440 | T | C | 1 | a0003c0006t0036g0196 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.137-10108T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813440 | |||||||
chr9:4813455 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0372 |
2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.137-10093C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813455 | |||||||
chr9:4813514 | C | T | 2 | a0001c0001t0013g0192 a0001c0004t0027g0193 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-10034C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813514 | |||||||
chr9:4813519 | C | A | 1 | a0001c0001t0001g0376 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.137-10029C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813519 | |||||||
chr9:4813593 | G | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0176 |
2 | NA18985.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.137-9955G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813593 | |||||||
chr9:4813726 | G | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-9822G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813726 | |||||||
chr9:4813751 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-9797C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813751 | |||||||
chr9:4813844 | A | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-9704A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813844 | |||||||
chr9:4813858 | A | T | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137-9690A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813858 | |||||||
chr9:4813900 | A | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-9648A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813900 | |||||||
chr9:4813932 | G | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0355 others(5): Show |
9 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-9616G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4813932 | |||||||
chr9:4814027 | G | A | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.137-9521G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814027 | |||||||
chr9:4814049 | G | A | 12 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(9): Show |
12 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.137-9499G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814049 | |||||||
chr9:4814110 | C | T | 1 | a0001c0007t0003g0238 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.137-9438C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814110 | |||||||
chr9:4814174 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-9374C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814174 | |||||||
chr9:4814213 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-9335C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814213 | |||||||
chr9:4814225 | T | TGAGGTGT others(284): Show |
3 | a0001c0001t0001g0042 a0001c0001t0003g0074 a0001c0001t0011g0055 |
3 | HG01361.hp2 HG03704.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.137-9307_137-9306i others(293): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814225 | T | TGAGGTGT others(285): Show |
2 | a0001c0001t0003g0080 a0001c0001t0005g0081 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.137-9307_137-9306i others(294): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814225 | T | TGAGGTGT others(285): Show |
35 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(32): Show |
35 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.137-9307_137-9306i others(294): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814225 | T | TGAGGTGT others(286): Show |
20 | a0001c0001t0001g0092 a0001c0001t0002g0067 a0001c0001t0002g0076 others(17): Show |
20 | HG00323.hp2 HG00621.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-9307_137-9306i others(295): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814225 | T | TGAGGTGT others(287): Show |
1 | a0001c0001t0003g0088 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.137-9307_137-9306i others(296): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814225 | T | TGAGGTGT others(288): Show |
1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.137-9307_137-9306i others(297): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4814225 | ||||||
chr9:4814253 | A | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-9295A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814253 | |||||||
chr9:4814293 | T | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-9255T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814293 | |||||||
chr9:4814319 | T | C | 92 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(89): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.137-9229T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814319 | |||||||
chr9:4814337 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.137-9211G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814337 | |||||||
chr9:4814470 | G | T | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137-9078G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814470 | |||||||
chr9:4814474 | C | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-9074C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814474 | |||||||
chr9:4814516 | C | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.137-9032C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814516 | |||||||
chr9:4814519 | G | A | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.137-9029G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814519 | |||||||
chr9:4814532 | G | T | 91 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(88): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-9016G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814532 | |||||||
chr9:4814631 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0014g0368 others(1): Show |
4 | HG03139.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-8917G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814631 | |||||||
chr9:4814635 | G | A | 133 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(130): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.137-8913G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814635 | |||||||
chr9:4814864 | A | G | 2 | a0001c0001t0012g0357 a0001c0001t0012g0358 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.137-8684A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814864 | |||||||
chr9:4814871 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.137-8677C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814871 | |||||||
chr9:4814900 | G | A | 40 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(37): Show |
40 | HG01074.hp2 HG01192.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.137-8648G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814900 | |||||||
chr9:4814928 | A | G | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.137-8620A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814928 | |||||||
chr9:4814948 | G | C | 104 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(101): Show |
106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.137-8600G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4814948 | |||||||
chr9:4815045 | C | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137-8503C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815045 | |||||||
chr9:4815094 | G | T | 1 | a0001c0001t0003g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.137-8454G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815094 | |||||||
chr9:4815154 | C | G | 2 | a0001c0001t0014g0368 a0001c0010t0001g0272 |
2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.137-8394C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815154 | |||||||
chr9:4815166 | C | G | 6 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(3): Show |
6 | NA18947.hp2 NA18954.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-8382C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815166 | |||||||
chr9:4815184 | A | G | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-8364A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815184 | |||||||
chr9:4815217 | TTCTCCTC others(3): Show |
T | 6 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-8330_137-8321d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815217 | |||||||
chr9:4815275 | T | A | 91 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(88): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-8273T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815275 | |||||||
chr9:4815427 | G | T | 8 | a0001c0001t0003g0088 a0001c0001t0006g0082 a0001c0001t0006g0083 others(5): Show |
8 | NA18951.hp1 NA18962.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-8121G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815427 | |||||||
chr9:4815453 | CT | C | 327 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(324): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.137-8083delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4815453 | ||||||
chr9:4815493 | G | C | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-8055G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815493 | |||||||
chr9:4815584 | G | A | 3 | a0001c0001t0017g0032 a0001c0001t0017g0033 a0001c0001t0017g0173 |
3 | NA18951.hp2 NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.137-7964G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815584 | |||||||
chr9:4815636 | C | G | 135 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(132): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.137-7912C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815636 | |||||||
chr9:4815648 | A | G | 91 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(88): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.137-7900A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815648 | |||||||
chr9:4815665 | C | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.137-7883C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815665 | |||||||
chr9:4815731 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-7817C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815731 | |||||||
chr9:4815735 | G | A | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7813G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815735 | |||||||
chr9:4815814 | G | A | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137-7734G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815814 | |||||||
chr9:4815863 | C | T | 2 | a0002c0002t0004g0198 a0002c0002t0028g0018 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.137-7685C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815863 | |||||||
chr9:4815938 | T | G | 4 | a0001c0001t0008g0202 a0001c0001t0008g0203 a0002c0002t0004g0198 others(1): Show |
4 | HG02055.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-7610T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815938 | |||||||
chr9:4815968 | G | T | 6 | a0001c0001t0001g0355 a0001c0001t0005g0353 a0001c0001t0008g0006 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7580G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4815968 | |||||||
chr9:4816184 | G | C | 41 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(38): Show |
41 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.137-7364G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816184 | |||||||
chr9:4816185 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0014g0368 others(2): Show |
5 | HG01243.hp2 HG03139.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-7363C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816185 | |||||||
chr9:4816349 | C | G | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0014g0194 others(4): Show |
7 | HG01243.hp2 HG01981.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-7199C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816349 | |||||||
chr9:4816396 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-7152G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816396 | |||||||
chr9:4816568 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0010 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.137-6980A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816568 | |||||||
chr9:4816581 | TTTTCCTT others(4): Show |
T | 1 | a0001c0001t0002g0338 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.137-6963_137-6953d others(13): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4816581 | ||||||
chr9:4816732 | A | G | 2 | a0002c0002t0004g0198 a0002c0002t0028g0018 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.137-6816A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816732 | |||||||
chr9:4816763 | A | G | 3 | a0001c0001t0013g0199 a0001c0001t0013g0366 a0001c0004t0027g0193 |
3 | HG02922.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.137-6785A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4816763 | |||||||
chr9:4817045 | C | G | 1 | a0002c0002t0014g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-6503C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817045 | |||||||
chr9:4817068 | C | T | 190 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.137-6480C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817068 | |||||||
chr9:4817069 | G | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-6479G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817069 | |||||||
chr9:4817146 | GA | G | 368 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(365): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.137-6394delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817146 | ||||||
chr9:4817321 | C | G | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-6227C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817321 | |||||||
chr9:4817374 | T | G | 326 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(323): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.137-6174T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817374 | |||||||
chr9:4817392 | C | G | 1 | a0001c0001t0014g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.137-6156C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817392 | |||||||
chr9:4817469 | AT | A | 327 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(324): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.137-6078delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817469 | |||||||
chr9:4817470 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.137-6078T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817470 | |||||||
chr9:4817470 | T | C | 51 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(48): Show |
52 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.137-6078T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817470 | |||||||
chr9:4817472 | T | C | 327 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(324): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.137-6076T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817472 | |||||||
chr9:4817530 | G | A | 2 | a0001c0001t0008g0360 a0001c0001t0008g0361 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-6018G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817530 | |||||||
chr9:4817577 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.137-5971G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817577 | |||||||
chr9:4817603 | A | C | 4 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0246 others(1): Show |
4 | HG00741.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5945A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817603 | |||||||
chr9:4817645 | C | T | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.137-5903C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817645 | |||||||
chr9:4817698 | T | G | 73 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0092 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.137-5850T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817698 | |||||||
chr9:4817859 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.137-5689T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817859 | |||||||
chr9:4817880 | C | A | 1 | a0001c0001t0013g0366 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137-5668C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817880 | |||||||
chr9:4817881 | T | A | 1 | a0001c0001t0013g0366 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137-5667T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817881 | |||||||
chr9:4817882 | C | T | 1 | a0001c0001t0013g0366 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.137-5666C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4817882 | |||||||
chr9:4817912 | A | AT | 20 | a0001c0001t0001g0300 a0001c0001t0001g0306 a0001c0001t0001g0307 others(17): Show |
20 | HG00735.hp1 HG00741.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.137-5611dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817912 | ||||||
chr9:4817912 | A | ATT | 147 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(144): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.137-5612_137-5611d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817912 | ||||||
chr9:4817912 | A | ATTT | 33 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0092 others(30): Show |
33 | HG00438.hp2 HG01109.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.137-5613_137-5611d others(5): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817912 | ||||||
chr9:4817912 | AT | A | 18 | a0001c0001t0002g0283 a0001c0001t0002g0285 a0001c0001t0003g0282 others(15): Show |
19 | HG00099.hp2 HG01081.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.137-5611delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817912 | ||||||
chr9:4817912 | ATTTTTT | A | 124 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(121): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.137-5616_137-5611d others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4817912 | ||||||
chr9:4818011 | C | T | 3 | a0001c0001t0001g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 |
3 | HG02055.hp2 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-5537C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818011 | |||||||
chr9:4818129 | C | T | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-5419C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818129 | |||||||
chr9:4818167 | C | T | 179 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(176): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.137-5381C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818167 | |||||||
chr9:4818201 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02258.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-5347A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818201 | |||||||
chr9:4818213 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137-5335G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818213 | |||||||
chr9:4818338 | C | G | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.137-5210C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818338 | |||||||
chr9:4818396 | A | G | 8 | a0001c0001t0001g0138 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG01993.hp2 HG02004.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-5152A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818396 | |||||||
chr9:4818403 | A | G | 90 | a0001c0001t0001g0070 a0001c0001t0001g0214 a0001c0001t0001g0217 others(87): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.137-5145A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818403 | |||||||
chr9:4818439 | A | C | 1 | a0001c0001t0014g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137-5109A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818439 | |||||||
chr9:4818441 | A | G | 1 | a0001c0001t0002g0259 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.137-5107A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818441 | |||||||
chr9:4818453 | G | C | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-5095G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818453 | |||||||
chr9:4818535 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.137-5013C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818535 | |||||||
chr9:4818544 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.137-5004G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818544 | |||||||
chr9:4818599 | C | A | 1 | a0001c0001t0014g0195 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.137-4949C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818599 | |||||||
chr9:4818607 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.137-4941G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818607 | |||||||
chr9:4818621 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.137-4927G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818621 | |||||||
chr9:4818657 | C | A | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.137-4891C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818657 | |||||||
chr9:4818694 | G | A | 132 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(129): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.137-4854G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818694 | |||||||
chr9:4818706 | C | G | 131 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(128): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.137-4842C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818706 | |||||||
chr9:4818809 | T | G | 2 | a0001c0001t0008g0202 a0001c0001t0008g0203 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.137-4739T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818809 | |||||||
chr9:4818812 | T | C | 326 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(323): Show |
330 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.137-4736T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818812 | |||||||
chr9:4818871 | CA | C | 248 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(245): Show |
251 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.137-4660delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4818871 | ||||||
chr9:4818871 | CAA | C | 17 | a0001c0001t0001g0070 a0001c0001t0001g0355 a0001c0001t0003g0007 others(14): Show |
18 | HG00733.hp1 HG01069.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.137-4661_137-4660d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4818871 | ||||||
chr9:4818872 | A | G | 1 | a0001c0001t0006g0319 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.137-4676A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4818872 | |||||||
chr9:4819002 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.137-4546A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819002 | |||||||
chr9:4819077 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.137-4471A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819077 | |||||||
chr9:4819166 | G | A | 8 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0364 others(5): Show |
8 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-4382G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819166 | |||||||
chr9:4819172 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0121 a0001c0001t0002g0022 others(3): Show |
6 | HG02027.hp2 HG02129.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-4376G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819172 | |||||||
chr9:4819237 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-4311C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819237 | |||||||
chr9:4819269 | A | C | 1 | a0001c0001t0008g0360 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.137-4279A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819269 | |||||||
chr9:4819282 | G | C | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.137-4266G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819282 | |||||||
chr9:4819380 | T | C | 2 | a0001c0001t0008g0202 a0001c0001t0008g0203 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.137-4168T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819380 | |||||||
chr9:4819421 | G | A | 129 | a0001c0001t0001g0037 a0001c0001t0001g0070 a0001c0001t0001g0106 others(126): Show |
130 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.137-4127G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819421 | |||||||
chr9:4819481 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0136 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.137-4067C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819481 | |||||||
chr9:4819572 | G | T | 1 | a0001c0001t0002g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.137-3976G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819572 | |||||||
chr9:4819598 | G | A | 4 | a0001c0001t0013g0192 a0001c0004t0027g0193 a0002c0002t0004g0198 others(1): Show |
4 | HG02886.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-3950G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819598 | |||||||
chr9:4819667 | C | T | 3 | a0001c0001t0010g0041 a0001c0001t0010g0144 a0001c0003t0002g0145 |
3 | NA19078.hp1 NA19078.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.137-3881C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819667 | |||||||
chr9:4819694 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-3854C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819694 | |||||||
chr9:4819732 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.137-3816G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819732 | |||||||
chr9:4819817 | A | G | 13 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(10): Show |
13 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-3731A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4819817 | |||||||
chr9:4820020 | G | A | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.137-3528G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820020 | |||||||
chr9:4820049 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.137-3499C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820049 | |||||||
chr9:4820080 | T | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.137-3468T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820080 | |||||||
chr9:4820355 | A | G | 1 | a0001c0001t0008g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.137-3193A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820355 | |||||||
chr9:4820438 | G | A | 174 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(171): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.137-3110G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820438 | |||||||
chr9:4820562 | A | T | 1 | a0001c0001t0002g0331 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.137-2986A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820562 | |||||||
chr9:4820606 | A | G | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137-2942A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820606 | |||||||
chr9:4820688 | A | T | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.137-2860A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820688 | |||||||
chr9:4820776 | A | C | 1 | a0002c0002t0014g0304 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.137-2772A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820776 | |||||||
chr9:4820870 | C | G | 7 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(4): Show |
8 | HG01109.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-2678C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820870 | |||||||
chr9:4820892 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0161 a0001c0001t0007g0040 others(7): Show |
10 | HG01081.hp2 HG01433.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-2656T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820892 | |||||||
chr9:4820999 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137-2549A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4820999 | |||||||
chr9:4821008 | A | G | 10 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(7): Show |
10 | HG01884.hp2 HG02145.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.137-2540A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821008 | |||||||
chr9:4821071 | T | C | 5 | a0001c0001t0003g0023 a0001c0001t0003g0056 a0001c0001t0003g0059 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-2477T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821071 | |||||||
chr9:4821308 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.137-2240A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821308 | |||||||
chr9:4821320 | T | C | 2 | a0001c0001t0008g0360 a0001c0001t0008g0361 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.137-2228T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821320 | |||||||
chr9:4821338 | T | G | 1 | a0001c0001t0005g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137-2210T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821338 | |||||||
chr9:4821348 | A | C | 95 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(92): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.137-2200A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821348 | |||||||
chr9:4821388 | G | C | 62 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0092 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.137-2160G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821388 | |||||||
chr9:4821388 | G | T | 1 | a0001c0001t0004g0050 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.137-2160G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821388 | |||||||
chr9:4821398 | G | T | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.137-2150G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821398 | |||||||
chr9:4821420 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-2128C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821420 | |||||||
chr9:4821452 | T | G | 352 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(349): Show |
357 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.137-2096T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821452 | |||||||
chr9:4821618 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.137-1930C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821618 | |||||||
chr9:4821644 | AT | A | 8 | a0001c0001t0001g0147 a0001c0001t0005g0353 a0001c0001t0008g0006 others(5): Show |
9 | HG00280.hp2 HG01099.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-1893delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4821644 | ||||||
chr9:4821655 | T | C | 94 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(91): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.137-1893T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821655 | |||||||
chr9:4821744 | G | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-1804G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821744 | |||||||
chr9:4821855 | T | C | 1 | a0001c0001t0015g0063 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.137-1693T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821855 | |||||||
chr9:4821878 | G | T | 6 | a0001c0001t0005g0353 a0001c0001t0008g0006 a0001c0001t0008g0351 others(3): Show |
7 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-1670G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4821878 | |||||||
chr9:4822151 | A | C | 1 | a0001c0001t0003g0181 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.137-1397A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822151 | |||||||
chr9:4822331 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.137-1217G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822331 | |||||||
chr9:4822521 | C | G | 325 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(322): Show |
329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.137-1027C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822521 | |||||||
chr9:4822589 | G | A | 2 | a0001c0001t0013g0192 a0001c0004t0027g0193 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.137-959G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822589 | |||||||
chr9:4822705 | C | T | 3 | a0001c0001t0002g0185 a0001c0001t0002g0222 a0001c0001t0002g0236 |
3 | NA19007.hp1 NA19066.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.137-843C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822705 | |||||||
chr9:4822775 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-773C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4822775 | |||||||
chr9:4823007 | G | T | 316 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(313): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.137-541G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823007 | |||||||
chr9:4823061 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.137-487C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823061 | |||||||
chr9:4823066 | A | C | 1 | a0001c0001t0002g0254 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.137-482A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823066 | |||||||
chr9:4823072 | A | G | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.137-476A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823072 | |||||||
chr9:4823154 | C | G | 2 | a0001c0001t0014g0194 a0001c0001t0014g0195 |
2 | HG01981.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.137-394C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823154 | |||||||
chr9:4823281 | AT | A | 46 | a0001c0001t0001g0092 a0001c0001t0001g0306 a0001c0001t0001g0307 others(43): Show |
48 | HG00099.hp2 HG00741.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.137-245delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4823281 | ||||||
chr9:4823281 | ATT | A | 177 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0070 others(174): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.137-246_137-245del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4823281 | ||||||
chr9:4823281 | ATTT | A | 139 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(136): Show |
141 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.137-247_137-245del others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 4823281 | ||||||
chr9:4823425 | G | T | 8 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(5): Show |
9 | HG00642.hp2 HG01516.hp1 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-123G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823425 | |||||||
chr9:4823456 | A | G | 13 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(10): Show |
13 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.137-92A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 1/8 | chr9 | 4823456 | |||||||
chr9:4823630 | T | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02896.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+11T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823630 | |||||||
chr9:4823680 | T | C | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.208+61T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823680 | |||||||
chr9:4823833 | A | C | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.208+214A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823833 | |||||||
chr9:4823837 | A | G | 1 | a0001c0001t0002g0221 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.208+218A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823837 | |||||||
chr9:4823840 | A | G | 1 | a0001c0001t0012g0344 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.208+221A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823840 | |||||||
chr9:4823846 | C | A | 1 | a0001c0001t0002g0242 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.208+227C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823846 | |||||||
chr9:4823881 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.208+262C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823881 | |||||||
chr9:4823955 | G | T | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.208+336G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4823955 | |||||||
chr9:4824003 | C | T | 67 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0092 others(64): Show |
67 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.208+384C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824003 | |||||||
chr9:4824218 | A | C | 1 | a0001c0001t0002g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208+599A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824218 | |||||||
chr9:4824252 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+633C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824252 | |||||||
chr9:4824259 | C | G | 1 | a0001c0001t0005g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.208+640C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824259 | |||||||
chr9:4824287 | C | A | 1 | a0001c0001t0003g0190 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.208+668C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824287 | |||||||
chr9:4824374 | A | AT | 157 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0070 others(154): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.208+776dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4824374 | ||||||
chr9:4824374 | A | ATT | 10 | a0001c0001t0001g0256 a0001c0001t0001g0262 a0001c0001t0002g0242 others(7): Show |
10 | HG00597.hp1 HG01109.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+775_208+776dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4824374 | ||||||
chr9:4824374 | AT | A | 12 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(9): Show |
12 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+776delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4824374 | ||||||
chr9:4824374 | ATT | A | 7 | a0001c0001t0002g0343 a0001c0001t0003g0318 a0001c0001t0005g0353 others(4): Show |
8 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+775_208+776del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4824374 | ||||||
chr9:4824374 | ATTT | A | 36 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(33): Show |
36 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.208+774_208+776del others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4824374 | ||||||
chr9:4824403 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+784C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824403 | |||||||
chr9:4824423 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.208+804C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824423 | |||||||
chr9:4824607 | G | T | 354 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(351): Show |
359 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.208+988G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824607 | |||||||
chr9:4824666 | C | T | 6 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+1047C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824666 | |||||||
chr9:4824685 | C | T | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.208+1066C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824685 | |||||||
chr9:4824686 | T | A | 7 | a0001c0001t0005g0353 a0001c0001t0008g0006 a0001c0001t0008g0351 others(4): Show |
8 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+1067T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824686 | |||||||
chr9:4824706 | C | A | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+1087C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824706 | |||||||
chr9:4824757 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+1138C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824757 | |||||||
chr9:4824764 | T | A | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.208+1145T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824764 | |||||||
chr9:4824840 | T | A | 2 | a0001c0001t0011g0244 a0001c0001t0011g0245 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.208+1221T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824840 | |||||||
chr9:4824967 | A | C | 40 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(37): Show |
40 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.208+1348A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824967 | |||||||
chr9:4824989 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+1370G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4824989 | |||||||
chr9:4825005 | G | A | 1 | a0001c0001t0035g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.208+1386G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825005 | |||||||
chr9:4825117 | G | A | 334 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(331): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.208+1498G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825117 | |||||||
chr9:4825129 | C | T | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.208+1510C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825129 | |||||||
chr9:4825176 | C | T | 4 | a0001c0001t0002g0188 a0001c0001t0021g0182 a0001c0001t0021g0183 others(1): Show |
4 | NA18975.hp1 NA18977.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1557C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825176 | |||||||
chr9:4825177 | G | T | 1 | a0001c0001t0002g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+1558G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825177 | |||||||
chr9:4825242 | G | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.209-1616G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825242 | |||||||
chr9:4825277 | G | C | 350 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(347): Show |
355 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.209-1581G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825277 | |||||||
chr9:4825296 | C | T | 2 | a0001c0001t0012g0357 a0001c0001t0012g0358 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.209-1562C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825296 | |||||||
chr9:4825541 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-1317C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825541 | |||||||
chr9:4825737 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA19009.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.209-1121A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825737 | |||||||
chr9:4825762 | G | A | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.209-1096G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825762 | |||||||
chr9:4825776 | G | T | 2 | a0001c0001t0001g0364 a0001c0001t0001g0365 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.209-1082G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825776 | |||||||
chr9:4825886 | T | C | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-972T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825886 | |||||||
chr9:4825930 | CA | C | 17 | a0001c0001t0001g0017 a0001c0001t0001g0275 a0001c0001t0001g0332 others(14): Show |
17 | HG01496.hp1 HG01928.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-916delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4825930 | ||||||
chr9:4825979 | C | T | 1 | a0001c0001t0008g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-879C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4825979 | |||||||
chr9:4826014 | G | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.209-844G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826014 | |||||||
chr9:4826078 | A | AAAAG | 11 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0364 others(8): Show |
11 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-760_209-757dup others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4826078 | ||||||
chr9:4826205 | C | T | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-653C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826205 | |||||||
chr9:4826219 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.209-639T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826219 | |||||||
chr9:4826363 | A | G | 5 | a0001c0001t0001g0300 a0001c0001t0001g0355 a0001c0001t0002g0298 others(2): Show |
5 | HG02257.hp1 HG03516.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-495A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826363 | |||||||
chr9:4826393 | A | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.209-465A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826393 | |||||||
chr9:4826403 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.209-455C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826403 | |||||||
chr9:4826459 | GC | G | 103 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0231 others(100): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.209-396delC | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 4826459 | ||||||
chr9:4826501 | T | A | 1 | a0001c0001t0003g0025 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.209-357T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826501 | |||||||
chr9:4826618 | C | T | 101 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0231 others(98): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.209-240C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826618 | |||||||
chr9:4826633 | T | C | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.209-225T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826633 | |||||||
chr9:4826663 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.209-195G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826663 | |||||||
chr9:4826690 | G | A | 1 | a0001c0001t0004g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.209-168G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826690 | |||||||
chr9:4826768 | G | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(35): Show |
38 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.209-90G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 2/8 | chr9 | 4826768 | |||||||
chr9:4827062 | G | A | 2 | a0002c0002t0004g0198 a0002c0002t0028g0018 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.384+29G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827062 | |||||||
chr9:4827082 | C | T | 3 | a0001c0001t0003g0108 a0001c0001t0020g0052 a0001c0001t0020g0053 |
3 | HG01361.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.384+49C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827082 | |||||||
chr9:4827107 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.384+74T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827107 | |||||||
chr9:4827194 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.384+161A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827194 | |||||||
chr9:4827217 | A | G | 12 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(9): Show |
12 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.384+184A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827217 | |||||||
chr9:4827222 | C | G | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.384+189C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827222 | |||||||
chr9:4827437 | G | A | 13 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(10): Show |
13 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.384+404G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827437 | |||||||
chr9:4827438 | C | T | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.384+405C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827438 | |||||||
chr9:4827439 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0014g0194 a0001c0001t0014g0195 |
3 | HG01981.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.384+406G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827439 | |||||||
chr9:4827449 | C | G | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+416C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827449 | |||||||
chr9:4827472 | C | G | 1 | a0001c0001t0004g0373 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.384+439C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827472 | |||||||
chr9:4827536 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.384+503G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827536 | |||||||
chr9:4827541 | T | C | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+508T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827541 | |||||||
chr9:4827637 | A | T | 175 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(172): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.384+604A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827637 | |||||||
chr9:4827719 | A | T | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+686A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827719 | |||||||
chr9:4827731 | A | AGT | 61 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0308 others(58): Show |
63 | HG00741.hp2 HG01074.hp2 HG01099.hp2 others(60): Show |
intron_variant | MODIFIER | c.384+722_384+723dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | A | AGTGT | 17 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0311 others(14): Show |
17 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.384+720_384+723dup others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | A | AGTGTGT | 9 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0246 others(6): Show |
9 | HG00280.hp1 HG00741.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.384+718_384+723dup others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | A | AGTGTGTG others(1): Show |
70 | a0001c0001t0001g0231 a0001c0001t0001g0257 a0001c0001t0001g0260 others(67): Show |
71 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.384+716_384+723dup others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | A | AGTGTGTG others(3): Show |
4 | a0001c0001t0002g0213 a0001c0001t0002g0223 a0001c0001t0002g0235 others(1): Show |
4 | HG03017.hp2 HG04204.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+714_384+723dup others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0002g0251 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.384+712_384+723dup others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | AGT | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0112 a0001c0001t0002g0076 others(8): Show |
11 | HG00733.hp1 HG01069.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.384+722_384+723del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827731 | AGTGT | A | 168 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(165): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.384+720_384+723del others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827731 | ||||||
chr9:4827751 | T | C | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+718T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827751 | |||||||
chr9:4827752 | G | A | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+719G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827752 | |||||||
chr9:4827753 | T | C | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+720T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827753 | |||||||
chr9:4827755 | T | C | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+722T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827755 | |||||||
chr9:4827756 | G | GTGTGCA | 4 | a0001c0001t0003g0326 a0001c0001t0012g0197 a0001c0001t0012g0344 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+723_384+724ins others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827756 | |||||||
chr9:4827757 | C | T | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+724C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827757 | |||||||
chr9:4827758 | A | G | 6 | a0001c0001t0001g0376 a0001c0001t0003g0059 a0001c0001t0003g0326 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+725A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827758 | |||||||
chr9:4827759 | C | T | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+726C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827759 | |||||||
chr9:4827761 | C | CGT | 98 | a0001c0001t0001g0214 a0001c0001t0001g0217 a0001c0001t0001g0231 others(95): Show |
99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.384+746_384+747dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827761 | ||||||
chr9:4827761 | C | CGTGT | 9 | a0001c0001t0002g0215 a0001c0001t0002g0220 a0001c0001t0002g0223 others(6): Show |
9 | HG00597.hp1 HG02165.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.384+744_384+747dup others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827761 | ||||||
chr9:4827761 | C | CGTGTGT | 168 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(165): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.384+742_384+747dup others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4827761 | ||||||
chr9:4827761 | C | T | 2 | a0001c0001t0001g0376 a0001c0001t0003g0059 |
2 | HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.384+728C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827761 | |||||||
chr9:4827763 | T | C | 33 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(30): Show |
33 | HG01074.hp2 HG01496.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.384+730T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827763 | |||||||
chr9:4827781 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.384+748A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827781 | |||||||
chr9:4827783 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.384+750A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827783 | |||||||
chr9:4827785 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.384+752A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827785 | |||||||
chr9:4827803 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.384+770T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827803 | |||||||
chr9:4827804 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.384+771C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827804 | |||||||
chr9:4827913 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.384+880G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827913 | |||||||
chr9:4827921 | T | G | 1 | a0001c0001t0002g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.384+888T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4827921 | |||||||
chr9:4828043 | A | G | 278 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.384+1010A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828043 | |||||||
chr9:4828103 | G | A | 2 | a0001c0001t0003g0318 a0001c0001t0003g0330 |
2 | NA19076.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.384+1070G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828103 | |||||||
chr9:4828161 | G | A | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0010g0224 |
3 | HG02602.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.384+1128G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828161 | |||||||
chr9:4828165 | C | CA | 28 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0112 others(25): Show |
28 | HG00140.hp1 HG01099.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.384+1156dupA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4828165 | ||||||
chr9:4828165 | CA | C | 22 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0311 others(19): Show |
22 | HG01074.hp1 HG01192.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.384+1156delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4828165 | ||||||
chr9:4828165 | CAAAAAAA others(3): Show |
C | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.384+1147_384+1156d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4828165 | ||||||
chr9:4828234 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.384+1201T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828234 | |||||||
chr9:4828354 | G | C | 4 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(1): Show |
4 | HG02630.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+1321G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828354 | |||||||
chr9:4828361 | A | T | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.384+1328A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828361 | |||||||
chr9:4828366 | G | A | 1 | a0001c0001t0002g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.384+1333G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828366 | |||||||
chr9:4828384 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.384+1351A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828384 | |||||||
chr9:4828399 | T | C | 1 | a0001c0001t0012g0357 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.384+1366T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828399 | |||||||
chr9:4828401 | C | A | 1 | a0001c0001t0006g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.384+1368C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828401 | |||||||
chr9:4828451 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.384+1418A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828451 | |||||||
chr9:4828470 | T | C | 2 | a0001c0001t0014g0194 a0001c0001t0014g0195 |
2 | HG01981.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.384+1437T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828470 | |||||||
chr9:4828546 | G | GT | 266 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(263): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.384+1526dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4828546 | ||||||
chr9:4828546 | G | GTT | 55 | a0001c0001t0001g0037 a0001c0001t0001g0092 a0001c0001t0001g0106 others(52): Show |
56 | HG00597.hp1 HG01074.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.384+1525_384+1526d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4828546 | ||||||
chr9:4828580 | G | C | 1 | a0001c0001t0002g0209 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.384+1547G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828580 | |||||||
chr9:4828647 | G | C | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+1614G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828647 | |||||||
chr9:4828874 | C | A | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.384+1841C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828874 | |||||||
chr9:4828881 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.384+1848A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4828881 | |||||||
chr9:4829016 | T | C | 1 | a0001c0001t0021g0183 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.384+1983T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829016 | |||||||
chr9:4829071 | C | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.384+2038C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829071 | |||||||
chr9:4829092 | G | A | 14 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(11): Show |
14 | HG01192.hp1 HG02055.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+2059G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829092 | |||||||
chr9:4829101 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+2068A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829101 | |||||||
chr9:4829188 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.384+2155C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829188 | |||||||
chr9:4829310 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.384+2277C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829310 | |||||||
chr9:4829487 | T | C | 322 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(319): Show |
326 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.384+2454T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829487 | |||||||
chr9:4829489 | G | T | 1 | a0005c0011t0031g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.384+2456G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829489 | |||||||
chr9:4829505 | G | T | 1 | a0005c0011t0031g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.384+2472G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829505 | |||||||
chr9:4829518 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.384+2485A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829518 | |||||||
chr9:4829535 | G | T | 1 | a0001c0001t0004g0373 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.384+2502G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829535 | |||||||
chr9:4829579 | G | T | 12 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(9): Show |
12 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.384+2546G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829579 | |||||||
chr9:4829669 | A | G | 1 | a0001c0001t0003g0091 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.384+2636A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829669 | |||||||
chr9:4829696 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.384+2663G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829696 | |||||||
chr9:4829790 | G | A | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.384+2757G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829790 | |||||||
chr9:4829803 | G | T | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384+2770G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829803 | |||||||
chr9:4829840 | A | T | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.384+2807A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829840 | |||||||
chr9:4829915 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.384+2882C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829915 | |||||||
chr9:4829928 | A | C | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.384+2895A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829928 | |||||||
chr9:4829970 | A | G | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384+2937A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829970 | |||||||
chr9:4829987 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384+2954G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4829987 | |||||||
chr9:4830338 | G | C | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.385-2816G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4830338 | |||||||
chr9:4830434 | TGAGCCTT others(3): Show |
T | 3 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0010g0224 |
3 | HG02602.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.385-2719_385-2710d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4830434 | |||||||
chr9:4830789 | C | G | 16 | a0001c0001t0002g0281 a0001c0001t0002g0283 a0001c0001t0002g0285 others(13): Show |
16 | HG00099.hp2 HG01081.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.385-2365C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4830789 | |||||||
chr9:4830849 | G | A | 302 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(299): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.385-2305G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4830849 | |||||||
chr9:4830893 | G | A | 2 | a0001c0001t0008g0202 a0001c0001t0008g0203 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.385-2261G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4830893 | |||||||
chr9:4831076 | A | C | 179 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(176): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.385-2078A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831076 | |||||||
chr9:4831198 | A | T | 1 | a0001c0001t0012g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.385-1956A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831198 | |||||||
chr9:4831291 | G | A | 1 | a0001c0001t0002g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.385-1863G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831291 | |||||||
chr9:4831329 | A | G | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.385-1825A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831329 | |||||||
chr9:4831330 | G | GAAAAAAA others(21): Show |
3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.385-1824_385-1823i others(30): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831330 | |||||||
chr9:4831332 | C | CAA | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.385-1822_385-1821i others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831332 | |||||||
chr9:4831333 | G | A | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.385-1821G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831333 | |||||||
chr9:4831640 | AT | A | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.385-1505delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4831640 | ||||||
chr9:4831898 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0003g0002 others(1): Show |
5 | NA18944.hp2 NA18962.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-1256G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831898 | |||||||
chr9:4831927 | C | G | 5 | a0001c0001t0005g0353 a0001c0001t0008g0006 a0001c0001t0008g0351 others(2): Show |
6 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-1227C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831927 | |||||||
chr9:4831953 | A | G | 278 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.385-1201A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4831953 | |||||||
chr9:4832005 | C | T | 3 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0060 |
3 | HG01106.hp1 HG01361.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.385-1149C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832005 | |||||||
chr9:4832130 | C | A | 328 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(325): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.385-1024C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832130 | |||||||
chr9:4832323 | A | G | 3 | a0001c0001t0003g0108 a0001c0001t0020g0052 a0001c0001t0020g0053 |
3 | HG01361.hp1 HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.385-831A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832323 | |||||||
chr9:4832421 | G | A | 3 | a0002c0002t0004g0198 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG02258.hp2 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.385-733G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832421 | |||||||
chr9:4832436 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.385-718C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832436 | |||||||
chr9:4832500 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.385-654A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832500 | |||||||
chr9:4832506 | A | G | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.385-648A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832506 | |||||||
chr9:4832618 | G | A | 93 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.385-536G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832618 | |||||||
chr9:4832623 | C | A | 1 | a0001c0001t0001g0374 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.385-531C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832623 | |||||||
chr9:4832624 | A | G | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.385-530A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832624 | |||||||
chr9:4832636 | C | T | 102 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(99): Show |
104 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.385-518C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832636 | |||||||
chr9:4832750 | G | C | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.385-404G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832750 | |||||||
chr9:4832765 | G | A | 1 | a0001c0001t0013g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.385-389G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832765 | |||||||
chr9:4832803 | C | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.385-351C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832803 | |||||||
chr9:4832805 | C | CA | 204 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(201): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.385-324dupA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4832805 | ||||||
chr9:4832805 | C | CAA | 18 | a0001c0001t0001g0117 a0001c0001t0001g0124 a0001c0001t0001g0160 others(15): Show |
18 | HG02040.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-325_385-324dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4832805 | ||||||
chr9:4832805 | CA | C | 8 | a0001c0001t0001g0274 a0001c0001t0003g0072 a0001c0001t0003g0088 others(5): Show |
8 | HG01928.hp1 HG02895.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-324delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4832805 | ||||||
chr9:4832805 | CAA | C | 5 | a0001c0001t0005g0353 a0001c0001t0008g0006 a0001c0001t0008g0351 others(2): Show |
6 | HG01099.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-325_385-324del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 4832805 | ||||||
chr9:4832888 | T | C | 278 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.385-266T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832888 | |||||||
chr9:4832911 | T | G | 278 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.385-243T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832911 | |||||||
chr9:4832931 | C | T | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.385-223C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832931 | |||||||
chr9:4832941 | A | G | 278 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.385-213A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832941 | |||||||
chr9:4832985 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.385-169A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4832985 | |||||||
chr9:4833086 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.385-68G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 3/8 | chr9 | 4833086 | |||||||
chr9:4833254 | T | G | 1 | a0001c0001t0009g0094 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.459+26T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833254 | |||||||
chr9:4833305 | A | G | 13 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(10): Show |
13 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+77A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833305 | |||||||
chr9:4833436 | G | A | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.459+208G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833436 | |||||||
chr9:4833437 | C | T | 171 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(168): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.459+209C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833437 | |||||||
chr9:4833545 | A | G | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+317A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833545 | |||||||
chr9:4833557 | T | C | 3 | a0001c0001t0001g0359 a0001c0001t0008g0360 a0001c0001t0008g0361 |
3 | HG02055.hp2 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.459+329T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833557 | |||||||
chr9:4833679 | T | A | 93 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(90): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.459+451T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833679 | |||||||
chr9:4833686 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0002g0005 a0001c0001t0002g0302 others(3): Show |
7 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-455A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833686 | |||||||
chr9:4833709 | G | C | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.460-432G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833709 | |||||||
chr9:4833777 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.460-364G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833777 | |||||||
chr9:4833794 | A | G | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.460-347A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833794 | |||||||
chr9:4833866 | T | C | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.460-275T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833866 | |||||||
chr9:4833960 | A | G | 309 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(306): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.460-181A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4833960 | |||||||
chr9:4834034 | A | G | 349 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(346): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.460-107A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4834034 | |||||||
chr9:4834079 | G | A | 10 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0002g0337 others(7): Show |
10 | HG01496.hp1 HG01993.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-62G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4834079 | |||||||
chr9:4834133 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18983.hp2 | splice_region_variant&intron_variant | LOW | c.460-8C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 4/8 | chr9 | 4834133 | |||||||
chr9:4834295 | T | C | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.584+30T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834295 | |||||||
chr9:4834299 | T | G | 99 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(96): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.584+34T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834299 | |||||||
chr9:4834299 | T | TG | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.584+34_584+35insG | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834299 | |||||||
chr9:4834332 | C | G | 1 | a0001c0001t0003g0190 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.584+67C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834332 | |||||||
chr9:4834394 | A | G | 327 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(324): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.584+129A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834394 | |||||||
chr9:4834420 | G | A | 12 | a0001c0001t0001g0311 a0001c0001t0001g0359 a0001c0001t0001g0363 others(9): Show |
12 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.584+155G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834420 | |||||||
chr9:4834438 | C | G | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.584+173C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834438 | |||||||
chr9:4834459 | G | A | 8 | a0001c0001t0002g0220 a0001c0001t0002g0223 a0001c0001t0002g0233 others(5): Show |
8 | HG00597.hp1 HG02165.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.584+194G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834459 | |||||||
chr9:4834471 | CT | C | 313 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(310): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.584+225delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 4834471 | ||||||
chr9:4834471 | CTT | C | 21 | a0001c0001t0001g0107 a0001c0001t0001g0138 a0001c0001t0001g0155 others(18): Show |
21 | HG00323.hp1 HG01074.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.584+224_584+225del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 4834471 | ||||||
chr9:4834551 | T | G | 1 | a0001c0001t0019g0027 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.584+286T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834551 | |||||||
chr9:4834597 | G | A | 310 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(307): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.584+332G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834597 | |||||||
chr9:4834689 | GAC | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0302 a0001c0001t0002g0303 others(1): Show |
5 | HG01109.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.584+426_584+427del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 4834689 | ||||||
chr9:4834707 | CT | C | 19 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(16): Show |
20 | HG00741.hp2 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.584+443delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834707 | |||||||
chr9:4834712 | G | A | 1 | a0001c0001t0006g0327 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.584+447G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834712 | |||||||
chr9:4834733 | A | G | 37 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(34): Show |
37 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(34): Show |
intron_variant | MODIFIER | c.584+468A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834733 | |||||||
chr9:4834814 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.584+549T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4834814 | |||||||
chr9:4835010 | G | A | 9 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+745G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835010 | |||||||
chr9:4835173 | G | A | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.584+908G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835173 | |||||||
chr9:4835219 | C | T | 9 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+954C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835219 | |||||||
chr9:4835245 | T | A | 42 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0324 others(39): Show |
42 | HG01074.hp2 HG01243.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.584+980T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835245 | |||||||
chr9:4835286 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.584+1021G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835286 | |||||||
chr9:4835371 | T | C | 9 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(6): Show |
9 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.584+1106T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835371 | |||||||
chr9:4835377 | T | G | 2 | a0001c0001t0001g0132 a0001c0001t0025g0126 |
2 | HG01074.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.584+1112T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835377 | |||||||
chr9:4835444 | T | G | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.584+1179T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835444 | |||||||
chr9:4835516 | C | T | 1 | a0001c0001t0003g0025 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.584+1251C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835516 | |||||||
chr9:4835521 | C | T | 28 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(25): Show |
29 | HG00741.hp2 HG01109.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.584+1256C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835521 | |||||||
chr9:4835574 | G | A | 102 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(99): Show |
104 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.584+1309G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835574 | |||||||
chr9:4835616 | A | G | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.584+1351A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835616 | |||||||
chr9:4835702 | C | T | 2 | a0001c0001t0001g0363 a0001c0001t0002g0362 |
2 | HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.584+1437C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835702 | |||||||
chr9:4835711 | C | T | 1 | a0001c0005t0004g0378 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.584+1446C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835711 | |||||||
chr9:4835717 | C | T | 254 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0024 others(251): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.584+1452C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835717 | |||||||
chr9:4835827 | C | G | 182 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(179): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.584+1562C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835827 | |||||||
chr9:4835835 | C | T | 1 | a0001c0001t0005g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.584+1570C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835835 | |||||||
chr9:4835895 | A | C | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.584+1630A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835895 | |||||||
chr9:4835910 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.584+1645G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4835910 | |||||||
chr9:4836009 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.584+1744C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836009 | |||||||
chr9:4836094 | G | T | 10 | a0001c0001t0001g0324 a0001c0001t0002g0321 a0001c0001t0002g0322 others(7): Show |
10 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.584+1829G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836094 | |||||||
chr9:4836103 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.584+1838A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836103 | |||||||
chr9:4836221 | A | G | 6 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0308 others(3): Show |
6 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+1956A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836221 | |||||||
chr9:4836246 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0023g0241 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.584+1981G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836246 | |||||||
chr9:4836274 | G | C | 24 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0002g0228 others(21): Show |
24 | HG01074.hp2 HG01243.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.584+2009G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836274 | |||||||
chr9:4836413 | C | T | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.584+2148C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836413 | |||||||
chr9:4836425 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.584+2160T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836425 | |||||||
chr9:4836447 | C | A | 3 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0060 |
3 | HG01106.hp1 HG01361.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.584+2182C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836447 | |||||||
chr9:4836454 | T | G | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.584+2189T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836454 | |||||||
chr9:4836566 | G | A | 93 | a0001c0001t0001g0151 a0001c0001t0001g0176 a0001c0001t0001g0231 others(90): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.584+2301G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836566 | |||||||
chr9:4836621 | C | T | 112 | a0001c0001t0001g0037 a0001c0001t0001g0113 a0001c0001t0001g0114 others(109): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.584+2356C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836621 | |||||||
chr9:4836640 | G | C | 87 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(84): Show |
87 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.584+2375G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836640 | |||||||
chr9:4836648 | G | T | 107 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0113 others(104): Show |
107 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.584+2383G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836648 | |||||||
chr9:4836656 | G | A | 25 | a0001c0001t0001g0017 a0001c0001t0001g0034 a0001c0001t0001g0092 others(22): Show |
25 | HG00741.hp2 HG01192.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.584+2391G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836656 | |||||||
chr9:4836811 | C | T | 172 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(169): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.584+2546C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836811 | |||||||
chr9:4836889 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG02896.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.584+2624A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836889 | |||||||
chr9:4836899 | A | C | 124 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(121): Show |
125 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.584+2634A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836899 | |||||||
chr9:4836918 | G | A | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.584+2653G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836918 | |||||||
chr9:4836935 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.584+2670G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4836935 | |||||||
chr9:4837126 | A | G | 1 | a0001c0001t0005g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.584+2861A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837126 | |||||||
chr9:4837144 | A | G | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.584+2879A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837144 | |||||||
chr9:4837260 | T | C | 118 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.584+2995T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837260 | |||||||
chr9:4837306 | C | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.584+3041C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837306 | |||||||
chr9:4837307 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.584+3042G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837307 | |||||||
chr9:4837317 | T | G | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.584+3052T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837317 | |||||||
chr9:4837324 | A | G | 1 | a0001c0001t0020g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.584+3059A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837324 | |||||||
chr9:4837486 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.584+3221T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837486 | |||||||
chr9:4837692 | G | C | 1 | a0001c0001t0002g0362 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.584+3427G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837692 | |||||||
chr9:4837743 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.584+3478A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837743 | |||||||
chr9:4837743 | A | G | 13 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0003g0088 others(10): Show |
13 | HG02027.hp2 NA18949.hp2 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.584+3478A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837743 | |||||||
chr9:4837768 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.585-3464A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837768 | |||||||
chr9:4837949 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.585-3283C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837949 | |||||||
chr9:4837954 | T | A | 1 | a0001c0001t0002g0380 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.585-3278T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837954 | |||||||
chr9:4837991 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0176 |
2 | HG02040.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.585-3241G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4837991 | |||||||
chr9:4838027 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.585-3205G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838027 | |||||||
chr9:4838108 | G | T | 1 | a0001c0001t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.585-3124G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838108 | |||||||
chr9:4838262 | G | A | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.585-2970G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838262 | |||||||
chr9:4838278 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.585-2954T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838278 | |||||||
chr9:4838321 | C | A | 4 | a0001c0001t0002g0356 a0001c0001t0011g0244 a0001c0001t0011g0245 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-2911C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838321 | |||||||
chr9:4838587 | TAC | T | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.585-2634_585-2633d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 4838587 | ||||||
chr9:4838682 | A | G | 1 | a0001c0001t0003g0345 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.585-2550A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838682 | |||||||
chr9:4838827 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.585-2405C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838827 | |||||||
chr9:4838861 | A | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.585-2371A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838861 | |||||||
chr9:4838929 | A | G | 10 | a0001c0001t0003g0025 a0001c0001t0003g0061 a0001c0001t0003g0062 others(7): Show |
10 | HG00621.hp1 HG02015.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.585-2303A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4838929 | |||||||
chr9:4839004 | A | G | 11 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(8): Show |
11 | HG01981.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.585-2228A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839004 | |||||||
chr9:4839221 | G | T | 1 | a0001c0001t0006g0039 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.585-2011G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839221 | |||||||
chr9:4839241 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG02896.hp2 HG02965.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.585-1991C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839241 | |||||||
chr9:4839412 | G | A | 4 | a0001c0001t0003g0326 a0001c0001t0012g0197 a0001c0001t0012g0344 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-1820G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839412 | |||||||
chr9:4839511 | T | C | 203 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.585-1721T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839511 | |||||||
chr9:4839553 | G | A | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.585-1679G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839553 | |||||||
chr9:4839627 | A | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-1605A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839627 | |||||||
chr9:4839892 | G | C | 3 | a0001c0005t0004g0378 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG01192.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.585-1340G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839892 | |||||||
chr9:4839926 | G | T | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-1306G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4839926 | |||||||
chr9:4840063 | C | T | 346 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(343): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.585-1169C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840063 | |||||||
chr9:4840076 | A | G | 2 | a0001c0001t0001g0364 a0001c0001t0001g0365 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.585-1156A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840076 | |||||||
chr9:4840125 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0001g0333 |
2 | NA18960.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.585-1107G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840125 | |||||||
chr9:4840380 | A | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-852A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840380 | |||||||
chr9:4840388 | TTGAAG | T | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.585-841_585-837del others(5): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 4840388 | ||||||
chr9:4840499 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.585-733A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840499 | |||||||
chr9:4840545 | G | T | 1 | a0001c0001t0001g0363 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.585-687G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840545 | |||||||
chr9:4840731 | G | C | 3 | a0001c0005t0004g0378 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG01192.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.585-501G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840731 | |||||||
chr9:4840740 | A | G | 3 | a0001c0005t0004g0378 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG01192.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.585-492A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840740 | |||||||
chr9:4840877 | G | A | 362 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(359): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.585-355G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840877 | |||||||
chr9:4840963 | G | A | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.585-269G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4840963 | |||||||
chr9:4841017 | C | G | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.585-215C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4841017 | |||||||
chr9:4841222 | C | T | 7 | a0001c0001t0008g0006 a0001c0001t0008g0269 a0001c0001t0008g0351 others(4): Show |
8 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.585-10C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 5/8 | chr9 | 4841222 | |||||||
chr9:4841368 | G | T | 7 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0004g0166 others(4): Show |
7 | HG01496.hp1 HG01993.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+11G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841368 | |||||||
chr9:4841503 | A | T | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+146A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841503 | |||||||
chr9:4841554 | A | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+197A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841554 | |||||||
chr9:4841667 | T | A | 73 | a0001c0001t0002g0076 a0001c0001t0002g0303 a0001c0001t0002g0305 others(70): Show |
74 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.710+310T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841667 | |||||||
chr9:4841699 | A | C | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+342A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841699 | |||||||
chr9:4841774 | T | A | 1 | a0001c0001t0006g0084 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.710+417T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841774 | |||||||
chr9:4841804 | C | T | 1 | a0001c0001t0005g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.710+447C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841804 | |||||||
chr9:4841877 | G | A | 346 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(343): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.710+520G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841877 | |||||||
chr9:4841892 | T | A | 2 | a0001c0001t0005g0064 a0001c0001t0005g0081 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.710+535T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841892 | |||||||
chr9:4841909 | C | G | 1 | a0001c0001t0002g0259 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.710+552C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841909 | |||||||
chr9:4841913 | G | A | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+556G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4841913 | |||||||
chr9:4842061 | T | C | 162 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0034 others(159): Show |
163 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.710+704T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842061 | |||||||
chr9:4842178 | C | A | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.710+821C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842178 | |||||||
chr9:4842378 | C | T | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.710+1021C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842378 | |||||||
chr9:4842408 | A | T | 1 | a0001c0001t0006g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.710+1051A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842408 | |||||||
chr9:4842670 | A | G | 363 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(360): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.710+1313A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842670 | |||||||
chr9:4842706 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.710+1349G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842706 | |||||||
chr9:4842773 | A | G | 342 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(339): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.710+1416A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842773 | |||||||
chr9:4842860 | T | C | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+1503T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842860 | |||||||
chr9:4842869 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.710+1512A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842869 | |||||||
chr9:4842891 | A | T | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.710+1534A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842891 | |||||||
chr9:4842967 | C | G | 92 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0117 others(89): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.711-1558C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4842967 | |||||||
chr9:4843094 | C | G | 1 | a0001c0001t0006g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.711-1431C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843094 | |||||||
chr9:4843154 | G | T | 3 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0192 |
3 | HG03209.hp2 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.711-1371G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843154 | |||||||
chr9:4843355 | C | A | 1 | a0001c0001t0006g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.711-1170C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843355 | |||||||
chr9:4843376 | A | AT | 103 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(100): Show |
104 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.711-1138dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 4843376 | ||||||
chr9:4843392 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.711-1133A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843392 | |||||||
chr9:4843536 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.711-989G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843536 | |||||||
chr9:4843599 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711-926C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843599 | |||||||
chr9:4843672 | C | G | 101 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(98): Show |
102 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.711-853C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843672 | |||||||
chr9:4843823 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.711-702T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843823 | |||||||
chr9:4843924 | G | C | 3 | a0001c0005t0004g0378 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG01192.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711-601G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4843924 | |||||||
chr9:4844051 | C | T | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-474C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844051 | |||||||
chr9:4844088 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.711-437C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844088 | |||||||
chr9:4844210 | G | C | 1 | a0001c0001t0010g0379 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.711-315G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844210 | |||||||
chr9:4844214 | T | C | 102 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(99): Show |
103 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.711-311T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844214 | |||||||
chr9:4844233 | C | T | 1 | a0001c0001t0006g0315 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.711-292C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844233 | |||||||
chr9:4844244 | G | A | 1 | a0001c0001t0003g0345 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.711-281G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844244 | |||||||
chr9:4844265 | T | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(93): Show |
97 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.711-260T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844265 | |||||||
chr9:4844387 | A | G | 1 | a0001c0001t0006g0084 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.711-138A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844387 | |||||||
chr9:4844459 | G | A | 152 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0117 others(149): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.711-66G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844459 | |||||||
chr9:4844473 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.711-52G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844473 | |||||||
chr9:4844507 | G | T | 355 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(352): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.711-18G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 6/8 | chr9 | 4844507 | |||||||
chr9:4844704 | T | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(93): Show |
97 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.867+23T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4844704 | |||||||
chr9:4844745 | C | G | 3 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0060 |
3 | HG01106.hp1 HG01361.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.867+64C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4844745 | |||||||
chr9:4844778 | A | C | 95 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(92): Show |
96 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.867+97A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4844778 | |||||||
chr9:4844866 | T | C | 2 | a0001c0001t0005g0353 a0001c0001t0035g0277 |
2 | HG01099.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.867+185T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4844866 | |||||||
chr9:4844934 | A | G | 1 | a0001c0001t0011g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.867+253A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4844934 | |||||||
chr9:4845007 | C | G | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.867+326C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845007 | |||||||
chr9:4845097 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.867+416C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845097 | |||||||
chr9:4845196 | T | C | 144 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0037 others(141): Show |
145 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.867+515T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845196 | |||||||
chr9:4845242 | G | A | 237 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0034 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.867+561G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845242 | |||||||
chr9:4845264 | A | G | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+583A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845264 | |||||||
chr9:4845360 | G | A | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.867+679G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845360 | |||||||
chr9:4845390 | T | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+709T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845390 | |||||||
chr9:4845520 | A | G | 95 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(92): Show |
96 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.867+839A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845520 | |||||||
chr9:4845540 | A | T | 11 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.867+859A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845540 | |||||||
chr9:4845585 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.867+904G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845585 | |||||||
chr9:4845717 | G | A | 1 | a0001c0001t0032g0187 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.867+1036G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845717 | |||||||
chr9:4845745 | G | T | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+1064G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845745 | |||||||
chr9:4845858 | T | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+1177T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4845858 | |||||||
chr9:4846070 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+1389A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846070 | |||||||
chr9:4846253 | A | G | 12 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(9): Show |
12 | HG01981.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.867+1572A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846253 | |||||||
chr9:4846290 | T | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+1609T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846290 | |||||||
chr9:4846327 | A | G | 15 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
15 | HG01192.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1646A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846327 | |||||||
chr9:4846445 | C | G | 143 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0117 others(140): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.867+1764C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846445 | |||||||
chr9:4846504 | T | G | 15 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
15 | HG01192.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1823T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846504 | |||||||
chr9:4846553 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.867+1872G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846553 | |||||||
chr9:4846568 | AG | A | 156 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0117 others(153): Show |
157 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.867+1893delG | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4846568 | ||||||
chr9:4846610 | T | C | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.867+1929T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846610 | |||||||
chr9:4846618 | T | G | 15 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(12): Show |
15 | HG01192.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.867+1937T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846618 | |||||||
chr9:4846642 | G | A | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.867+1961G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846642 | |||||||
chr9:4846834 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.867+2153G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846834 | |||||||
chr9:4846894 | C | CTTTTTTC others(1): Show |
92 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0029 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.867+2219_867+2220i others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4846894 | ||||||
chr9:4846894 | C | CTTTTTTC others(8): Show |
250 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0034 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.867+2219_867+2220i others(17): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4846894 | ||||||
chr9:4846894 | C | CTTTTTTC others(9): Show |
1 | a0001c0001t0003g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.867+2219_867+2220i others(18): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4846894 | ||||||
chr9:4846894 | C | CTTTTTTC others(8): Show |
1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+2219_867+2220i others(17): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4846894 | ||||||
chr9:4846894 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.867+2213C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846894 | |||||||
chr9:4846901 | T | C | 1 | a0001c0001t0002g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.867+2220T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4846901 | |||||||
chr9:4847168 | T | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(93): Show |
97 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.868-2279T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847168 | |||||||
chr9:4847172 | C | G | 83 | a0001c0001t0001g0324 a0001c0001t0002g0005 a0001c0001t0002g0076 others(80): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.868-2275C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847172 | |||||||
chr9:4847304 | A | G | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.868-2143A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847304 | |||||||
chr9:4847538 | G | A | 1 | a0001c0001t0003g0335 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.868-1909G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847538 | |||||||
chr9:4847570 | T | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(93): Show |
97 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.868-1877T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847570 | |||||||
chr9:4847637 | T | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0260 a0001c0001t0001g0263 |
3 | NA18988.hp1 NA19000.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.868-1810T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847637 | |||||||
chr9:4847933 | A | T | 3 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0192 |
3 | HG03209.hp2 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.868-1514A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847933 | |||||||
chr9:4847957 | G | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.868-1490G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4847957 | |||||||
chr9:4848205 | G | A | 3 | a0001c0005t0004g0378 a0002c0002t0014g0304 a0002c0002t0028g0018 |
3 | HG01192.hp1 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.868-1242G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848205 | |||||||
chr9:4848297 | A | G | 95 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(92): Show |
96 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.868-1150A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848297 | |||||||
chr9:4848357 | A | T | 155 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0034 others(152): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.868-1090A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848357 | |||||||
chr9:4848448 | A | C | 1 | a0001c0001t0001g0367 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.868-999A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848448 | |||||||
chr9:4848518 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.868-929G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848518 | |||||||
chr9:4848630 | A | G | 70 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0002g0076 others(67): Show |
71 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.868-817A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848630 | |||||||
chr9:4848724 | A | G | 2 | a0001c0001t0003g0002 a0001c0001t0003g0131 |
3 | NA18944.hp2 NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.868-723A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848724 | |||||||
chr9:4848845 | A | G | 1 | a0001c0001t0009g0170 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.868-602A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848845 | |||||||
chr9:4848860 | A | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0349 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.868-587A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848860 | |||||||
chr9:4848875 | G | T | 345 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(342): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.868-572G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4848875 | |||||||
chr9:4849027 | C | A | 13 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(10): Show |
13 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.868-420C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849027 | |||||||
chr9:4849040 | C | T | 1 | a0001c0001t0014g0368 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.868-407C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849040 | |||||||
chr9:4849054 | C | A | 1 | a0001c0001t0001g0300 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.868-393C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849054 | |||||||
chr9:4849093 | A | AT | 173 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0028 others(170): Show |
174 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.868-341dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4849093 | ||||||
chr9:4849093 | A | ATT | 9 | a0001c0001t0001g0363 a0001c0001t0001g0365 a0001c0001t0001g0367 others(6): Show |
9 | HG01981.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.868-342_868-341dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4849093 | ||||||
chr9:4849107 | G | T | 68 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0002g0076 others(65): Show |
69 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.868-340G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849107 | |||||||
chr9:4849168 | AT | A | 258 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(255): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.868-264delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4849168 | ||||||
chr9:4849168 | ATT | A | 11 | a0001c0001t0001g0017 a0001c0001t0002g0298 a0001c0001t0002g0299 others(8): Show |
11 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.868-265_868-264del others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 4849168 | ||||||
chr9:4849313 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.868-134C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849313 | |||||||
chr9:4849379 | T | C | 1 | a0001c0001t0003g0345 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.868-68T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 7/8 | chr9 | 4849379 | |||||||
chr9:4849647 | T | C | 96 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(93): Show |
97 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.971+97T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4849647 | |||||||
chr9:4849653 | C | G | 1 | a0001c0001t0018g0294 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.971+103C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4849653 | |||||||
chr9:4849668 | C | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.971+118C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4849668 | |||||||
chr9:4849907 | G | T | 9 | a0001c0001t0001g0324 a0001c0001t0002g0005 a0001c0001t0002g0302 others(6): Show |
10 | HG01109.hp2 HG02622.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.971+357G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4849907 | |||||||
chr9:4849951 | C | A | 1 | a0001c0001t0003g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.971+401C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4849951 | |||||||
chr9:4850141 | T | C | 142 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0157 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.971+591T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850141 | |||||||
chr9:4850213 | C | T | 2 | a0001c0001t0001g0364 a0001c0001t0001g0365 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.971+663C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850213 | |||||||
chr9:4850406 | C | T | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+856C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850406 | |||||||
chr9:4850421 | C | G | 349 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.971+871C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850421 | |||||||
chr9:4850431 | A | G | 146 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0037 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.971+881A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850431 | |||||||
chr9:4850436 | G | T | 203 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.971+886G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850436 | |||||||
chr9:4850490 | T | TTTTC | 85 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(82): Show |
86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.971+942_971+943ins others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4850490 | ||||||
chr9:4850493 | C | CT | 23 | a0001c0001t0002g0204 a0001c0001t0002g0208 a0001c0001t0002g0209 others(20): Show |
23 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.971+960dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4850493 | ||||||
chr9:4850493 | C | CTT | 73 | a0001c0001t0001g0324 a0001c0001t0001g0332 a0001c0001t0001g0333 others(70): Show |
75 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.971+959_971+960dup others(2): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4850493 | ||||||
chr9:4850493 | C | CTTT | 34 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(31): Show |
35 | HG01243.hp1 HG01891.hp2 HG01981.hp1 others(32): Show |
intron_variant | MODIFIER | c.971+958_971+960dup others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4850493 | ||||||
chr9:4850493 | C | T | 92 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.971+943C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850493 | |||||||
chr9:4850499 | T | C | 2 | a0001c0001t0013g0199 a0001c0001t0013g0366 |
2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.971+949T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850499 | |||||||
chr9:4850505 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.971+955T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850505 | |||||||
chr9:4850613 | A | G | 202 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.971+1063A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850613 | |||||||
chr9:4850646 | G | A | 6 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.971+1096G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850646 | |||||||
chr9:4850716 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.971+1166T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850716 | |||||||
chr9:4850774 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0134 |
2 | NA18952.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.971+1224G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850774 | |||||||
chr9:4850820 | A | G | 1 | a0001c0003t0016g0046 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.971+1270A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850820 | |||||||
chr9:4850854 | A | T | 1 | a0001c0001t0002g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.971+1304A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850854 | |||||||
chr9:4850872 | C | T | 1 | a0001c0001t0002g0251 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.971+1322C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850872 | |||||||
chr9:4850876 | T | C | 146 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0037 others(143): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.971+1326T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850876 | |||||||
chr9:4850896 | C | T | 2 | a0002c0002t0014g0304 a0002c0002t0028g0018 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.971+1346C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850896 | |||||||
chr9:4850972 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0155 |
2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.971+1422G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4850972 | |||||||
chr9:4851008 | A | C | 12 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0324 others(9): Show |
13 | HG01109.hp2 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.971+1458A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851008 | |||||||
chr9:4851105 | C | T | 1 | a0001c0001t0001g0376 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.971+1555C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851105 | |||||||
chr9:4851132 | T | C | 1 | a0001c0001t0001g0363 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.971+1582T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851132 | |||||||
chr9:4851157 | T | G | 3 | a0001c0001t0003g0075 a0001c0001t0003g0093 a0001c0001t0003g0377 |
3 | HG00099.hp1 HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.971+1607T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851157 | |||||||
chr9:4851328 | G | A | 12 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(9): Show |
12 | HG01981.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.971+1778G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851328 | |||||||
chr9:4851401 | G | A | 3 | a0001c0001t0002g0253 a0001c0001t0002g0254 a0001c0001t0010g0379 |
3 | HG04199.hp1 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.971+1851G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851401 | |||||||
chr9:4851433 | C | G | 1 | a0001c0001t0002g0235 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.971+1883C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851433 | |||||||
chr9:4851440 | A | G | 339 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(336): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.971+1890A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851440 | |||||||
chr9:4851460 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.971+1910C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851460 | |||||||
chr9:4851461 | A | G | 349 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.971+1911A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851461 | |||||||
chr9:4851464 | A | G | 349 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.971+1914A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851464 | |||||||
chr9:4851515 | A | G | 149 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0157 others(146): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.971+1965A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851515 | |||||||
chr9:4851540 | A | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.971+1990A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851540 | |||||||
chr9:4851588 | A | G | 21 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0324 others(18): Show |
23 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.971+2038A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851588 | |||||||
chr9:4851661 | T | C | 349 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(346): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.971+2111T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851661 | |||||||
chr9:4851737 | T | TA | 143 | a0001c0001t0001g0117 a0001c0001t0001g0129 a0001c0001t0001g0157 others(140): Show |
144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.971+2199dupA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851737 | ||||||
chr9:4851737 | T | TAA | 198 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(195): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.971+2198_971+2199d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851737 | ||||||
chr9:4851737 | T | TAAA | 7 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+2197_971+2199d others(5): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851737 | ||||||
chr9:4851867 | G | A | 12 | a0001c0001t0001g0311 a0001c0001t0001g0363 a0001c0001t0001g0364 others(9): Show |
12 | HG01981.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.971+2317G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851867 | |||||||
chr9:4851885 | C | CTTTTTT | 141 | a0001c0001t0001g0028 a0001c0001t0001g0117 a0001c0001t0001g0129 others(138): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.971+2343_971+2348d others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851885 | ||||||
chr9:4851885 | C | CTTTTTTT | 129 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0024 others(126): Show |
132 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.971+2342_971+2348d others(9): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851885 | ||||||
chr9:4851885 | C | CTTTTTTT others(1): Show |
63 | a0001c0001t0001g0021 a0001c0001t0001g0036 a0001c0001t0001g0111 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.971+2341_971+2348d others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851885 | ||||||
chr9:4851885 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0003g0054 a0001c0001t0003g0059 a0001c0001t0003g0119 others(10): Show |
13 | HG00735.hp1 HG01081.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.971+2340_971+2348d others(11): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851885 | ||||||
chr9:4851885 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0139 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.971+2339_971+2348d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4851885 | ||||||
chr9:4851888 | T | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0355 |
2 | HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.971+2338T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851888 | |||||||
chr9:4851919 | C | T | 237 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0117 others(234): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.971+2369C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851919 | |||||||
chr9:4851933 | G | T | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.971+2383G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851933 | |||||||
chr9:4851966 | C | T | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.971+2416C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851966 | |||||||
chr9:4851976 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.971+2426G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851976 | |||||||
chr9:4851983 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.971+2433G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4851983 | |||||||
chr9:4852106 | C | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0103 a0001c0001t0001g0105 others(1): Show |
4 | NA18952.hp2 NA18983.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+2556C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852106 | |||||||
chr9:4852386 | C | A | 4 | a0001c0001t0003g0326 a0001c0001t0012g0197 a0001c0001t0012g0344 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+2836C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852386 | |||||||
chr9:4852538 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0216 a0001c0001t0002g0232 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+2988G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852538 | |||||||
chr9:4852599 | A | G | 100 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.971+3049A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852599 | |||||||
chr9:4852640 | C | A | 11 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(8): Show |
11 | HG02559.hp2 HG02622.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+3090C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852640 | |||||||
chr9:4852728 | A | C | 164 | a0001c0001t0001g0034 a0001c0001t0001g0157 a0001c0001t0001g0174 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.971+3178A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852728 | |||||||
chr9:4852732 | C | T | 164 | a0001c0001t0001g0034 a0001c0001t0001g0157 a0001c0001t0001g0174 others(161): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.971+3182C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852732 | |||||||
chr9:4852769 | C | CT | 232 | a0001c0001t0001g0034 a0001c0001t0001g0157 a0001c0001t0001g0174 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.971+3233dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4852769 | ||||||
chr9:4852769 | C | CTT | 100 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(97): Show |
101 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.971+3232_971+3233d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4852769 | ||||||
chr9:4852820 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.971+3270G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4852820 | |||||||
chr9:4853073 | G | A | 1 | a0001c0001t0007g0043 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.971+3523G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853073 | |||||||
chr9:4853114 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.971+3564G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853114 | |||||||
chr9:4853160 | T | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.971+3610T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853160 | |||||||
chr9:4853171 | A | G | 1 | a0001c0001t0007g0045 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.971+3621A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853171 | |||||||
chr9:4853179 | C | T | 140 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(137): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.971+3629C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853179 | |||||||
chr9:4853187 | A | G | 15 | a0001c0001t0001g0217 a0001c0001t0001g0246 a0001c0001t0001g0311 others(12): Show |
15 | HG00741.hp1 HG01981.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.971+3637A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853187 | |||||||
chr9:4853198 | C | T | 63 | a0001c0001t0002g0076 a0001c0001t0003g0002 a0001c0001t0003g0007 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.971+3648C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853198 | |||||||
chr9:4853232 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.971+3682G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853232 | |||||||
chr9:4853324 | C | CT | 10 | a0001c0001t0001g0164 a0001c0001t0002g0229 a0001c0001t0002g0252 others(7): Show |
10 | HG01192.hp2 HG01433.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.971+3791dupT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4853324 | ||||||
chr9:4853324 | C | CTT | 23 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(20): Show |
25 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.971+3790_971+3791d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4853324 | ||||||
chr9:4853324 | CT | C | 85 | a0001c0001t0001g0217 a0001c0001t0001g0246 a0001c0001t0001g0363 others(82): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.971+3791delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4853324 | ||||||
chr9:4853346 | C | T | 4 | a0001c0001t0003g0119 a0001c0001t0003g0137 a0001c0001t0003g0139 others(1): Show |
4 | HG02922.hp2 NA18956.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+3796C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853346 | |||||||
chr9:4853389 | T | A | 1 | a0001c0001t0002g0227 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.971+3839T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853389 | |||||||
chr9:4853514 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.971+3964G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853514 | |||||||
chr9:4853528 | A | C | 6 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0192 others(3): Show |
6 | HG01981.hp1 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+3978A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853528 | |||||||
chr9:4853682 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.971+4132T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853682 | |||||||
chr9:4853728 | G | A | 3 | a0001c0001t0005g0064 a0001c0001t0005g0081 a0001c0001t0005g0293 |
3 | HG01168.hp2 HG01169.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.971+4178G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853728 | |||||||
chr9:4853751 | A | C | 1 | a0001c0005t0001g0350 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.971+4201A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853751 | |||||||
chr9:4853751 | A | G | 99 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(96): Show |
100 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.971+4201A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853751 | |||||||
chr9:4853793 | CT | C | 65 | a0001c0001t0002g0076 a0001c0001t0003g0002 a0001c0001t0003g0007 others(62): Show |
66 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.971+4253delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4853793 | ||||||
chr9:4853830 | A | G | 11 | a0001c0001t0003g0088 a0001c0001t0003g0190 a0001c0001t0006g0039 others(8): Show |
11 | HG00438.hp2 HG02027.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.971+4280A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853830 | |||||||
chr9:4853862 | A | G | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.971+4312A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853862 | |||||||
chr9:4853887 | G | T | 24 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(21): Show |
26 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.971+4337G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853887 | |||||||
chr9:4853984 | C | G | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0011g0244 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.971+4434C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853984 | |||||||
chr9:4853986 | A | G | 4 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0261 others(1): Show |
4 | NA18947.hp2 NA18985.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+4436A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4853986 | |||||||
chr9:4854055 | C | T | 1 | a0002c0002t0004g0198 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.971+4505C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854055 | |||||||
chr9:4854110 | G | A | 1 | a0001c0001t0003g0336 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.971+4560G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854110 | |||||||
chr9:4854115 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.971+4565T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854115 | |||||||
chr9:4854148 | T | C | 1 | a0001c0001t0003g0375 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.971+4598T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854148 | |||||||
chr9:4854253 | C | T | 9 | a0001c0001t0001g0070 a0001c0001t0001g0132 a0001c0001t0001g0146 others(6): Show |
9 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+4703C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854253 | |||||||
chr9:4854265 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.971+4715A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854265 | |||||||
chr9:4854307 | A | G | 141 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(138): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.971+4757A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854307 | |||||||
chr9:4854433 | T | C | 141 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(138): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.971+4883T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854433 | |||||||
chr9:4854472 | C | G | 73 | a0001c0001t0001g0157 a0001c0001t0001g0255 a0001c0001t0001g0256 others(70): Show |
74 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.971+4922C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854472 | |||||||
chr9:4854484 | G | T | 1 | a0001c0001t0034g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.971+4934G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854484 | |||||||
chr9:4854516 | C | T | 1 | a0001c0010t0001g0272 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.971+4966C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854516 | |||||||
chr9:4854586 | C | T | 137 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(134): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.971+5036C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854586 | |||||||
chr9:4854678 | T | C | 140 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(137): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.971+5128T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854678 | |||||||
chr9:4854823 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.971+5273G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854823 | |||||||
chr9:4854882 | C | T | 137 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(134): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.972-5243C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4854882 | |||||||
chr9:4855061 | A | AC | 20 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0324 others(17): Show |
22 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.972-5064_972-5063i others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855061 | |||||||
chr9:4855062 | A | AC | 5 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0192 others(2): Show |
5 | HG01981.hp1 HG02572.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.972-5063_972-5062i others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855062 | |||||||
chr9:4855065 | A | AC | 21 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0174 others(18): Show |
21 | HG00741.hp1 HG01243.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.972-5060_972-5059i others(3): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855065 | |||||||
chr9:4855065 | A | C | 189 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(186): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.972-5060A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855065 | |||||||
chr9:4855072 | A | AAAAAAC | 18 | a0001c0001t0001g0266 a0001c0001t0002g0004 a0001c0001t0002g0188 others(15): Show |
18 | HG01099.hp1 HG01256.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.972-5052_972-5051i others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4855072 | ||||||
chr9:4855072 | A | AAAAAC | 90 | a0001c0001t0001g0157 a0001c0001t0001g0255 a0001c0001t0001g0256 others(87): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.972-5052_972-5051i others(7): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4855072 | ||||||
chr9:4855072 | A | AAAAC | 31 | a0001c0001t0001g0214 a0001c0001t0001g0306 a0001c0001t0001g0307 others(28): Show |
31 | HG00741.hp2 HG01099.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.972-5052_972-5051i others(6): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4855072 | ||||||
chr9:4855072 | A | C | 210 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(207): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.972-5053A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855072 | |||||||
chr9:4855074 | T | A | 1 | a0001c0001t0002g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.972-5051T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855074 | |||||||
chr9:4855226 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.972-4899T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855226 | |||||||
chr9:4855268 | C | G | 1 | a0001c0001t0004g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.972-4857C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855268 | |||||||
chr9:4855306 | T | A | 10 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(7): Show |
11 | HG00642.hp2 HG01516.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.972-4819T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855306 | |||||||
chr9:4855309 | G | A | 140 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(137): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.972-4816G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855309 | |||||||
chr9:4855362 | G | GTC | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.972-4759_972-4758d others(4): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4855362 | ||||||
chr9:4855514 | C | A | 321 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.972-4611C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855514 | |||||||
chr9:4855620 | G | C | 1 | a0001c0001t0001g0374 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.972-4505G>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855620 | |||||||
chr9:4855781 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0011g0244 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-4344G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855781 | |||||||
chr9:4855858 | A | C | 103 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(100): Show |
105 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.972-4267A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855858 | |||||||
chr9:4855912 | C | T | 207 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(204): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.972-4213C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855912 | |||||||
chr9:4855939 | C | T | 1 | a0001c0008t0026g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.972-4186C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4855939 | |||||||
chr9:4856019 | C | G | 345 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(342): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.972-4106C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856019 | |||||||
chr9:4856097 | T | G | 2 | a0001c0001t0001g0369 a0001c0001t0001g0371 |
2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.972-4028T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856097 | |||||||
chr9:4856216 | G | A | 7 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0230 others(4): Show |
7 | HG00323.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.972-3909G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856216 | |||||||
chr9:4856234 | G | A | 208 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.972-3891G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856234 | |||||||
chr9:4856339 | G | T | 137 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(134): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.972-3786G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856339 | |||||||
chr9:4856417 | A | G | 208 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.972-3708A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856417 | |||||||
chr9:4856457 | A | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.972-3668A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856457 | |||||||
chr9:4856568 | T | G | 348 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(345): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.972-3557T>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856568 | |||||||
chr9:4856591 | A | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG02896.hp2 HG02965.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-3534A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856591 | |||||||
chr9:4856724 | G | A | 136 | a0001c0001t0001g0157 a0001c0001t0001g0214 a0001c0001t0001g0255 others(133): Show |
137 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.972-3401G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856724 | |||||||
chr9:4856877 | G | A | 93 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(90): Show |
94 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.972-3248G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4856877 | |||||||
chr9:4857410 | G | A | 2 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.972-2715G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857410 | |||||||
chr9:4857428 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.972-2697G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857428 | |||||||
chr9:4857437 | C | G | 1 | a0001c0001t0001g0371 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.972-2688C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857437 | |||||||
chr9:4857443 | T | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0011g0244 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-2682T>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857443 | |||||||
chr9:4857458 | GA | G | 195 | a0001c0001t0001g0034 a0001c0001t0001g0157 a0001c0001t0001g0174 others(192): Show |
198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.972-2656delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857458 | ||||||
chr9:4857563 | T | C | 2 | a0001c0001t0005g0064 a0001c0001t0005g0081 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.972-2562T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857563 | |||||||
chr9:4857643 | G | A | 2 | a0001c0003t0002g0019 a0001c0003t0002g0145 |
2 | NA18953.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.972-2482G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857643 | |||||||
chr9:4857662 | C | T | 360 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(357): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.972-2463C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857662 | |||||||
chr9:4857712 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.972-2413G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857712 | |||||||
chr9:4857802 | C | T | 173 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.972-2323C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857802 | |||||||
chr9:4857859 | A | G | 1 | a0001c0001t0001g0365 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.972-2266A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857859 | |||||||
chr9:4857931 | C | CTTTTTT | 25 | a0001c0001t0001g0217 a0001c0001t0001g0246 a0001c0001t0001g0311 others(22): Show |
26 | HG00741.hp1 HG01099.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.972-2180_972-2175d others(8): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | C | CTTTTTTT | 31 | a0001c0001t0001g0214 a0001c0001t0001g0306 a0001c0001t0001g0307 others(28): Show |
31 | HG00741.hp2 HG01069.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.972-2181_972-2175d others(9): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | C | CTTTTTTT others(1): Show |
125 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.972-2182_972-2175d others(10): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | C | CTTTTTTT others(2): Show |
33 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(30): Show |
33 | HG00621.hp2 HG00735.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.972-2183_972-2175d others(11): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0007g0048 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.972-2184_972-2175d others(12): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | CT | C | 112 | a0001c0001t0001g0157 a0001c0001t0001g0255 a0001c0001t0001g0256 others(109): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.972-2175delT | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857931 | CTTTTTTT | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.972-2181_972-2175d others(9): Show |
RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | 4857931 | ||||||
chr9:4857951 | C | T | 9 | a0001c0001t0008g0006 a0001c0001t0008g0202 a0001c0001t0008g0203 others(6): Show |
10 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-2174C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4857951 | |||||||
chr9:4858011 | C | G | 8 | a0001c0001t0002g0223 a0001c0001t0002g0233 a0001c0001t0002g0234 others(5): Show |
8 | NA18940.hp1 NA18944.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-2114C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858011 | |||||||
chr9:4858019 | A | G | 228 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(225): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.972-2106A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858019 | |||||||
chr9:4858107 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.972-2018C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858107 | |||||||
chr9:4858114 | A | G | 228 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(225): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.972-2011A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858114 | |||||||
chr9:4858234 | A | G | 1 | a0001c0001t0034g0102 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.972-1891A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858234 | |||||||
chr9:4858253 | C | G | 43 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0175 others(40): Show |
43 | HG00741.hp2 HG01099.hp2 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.972-1872C>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858253 | |||||||
chr9:4858266 | T | C | 1 | a0001c0001t0004g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.972-1859T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858266 | |||||||
chr9:4858430 | G | A | 1 | a0002c0002t0028g0018 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.972-1695G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858430 | |||||||
chr9:4858433 | G | A | 11 | a0001c0001t0008g0006 a0001c0001t0008g0202 a0001c0001t0008g0203 others(8): Show |
12 | HG01192.hp1 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.972-1692G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858433 | |||||||
chr9:4858542 | G | A | 3 | a0001c0001t0011g0055 a0001c0001t0011g0057 a0001c0001t0011g0060 |
3 | HG01106.hp1 HG01361.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.972-1583G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858542 | |||||||
chr9:4858616 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.972-1509A>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858616 | |||||||
chr9:4858676 | A | G | 1 | a0001c0004t0027g0193 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.972-1449A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858676 | |||||||
chr9:4858694 | A | G | 62 | a0001c0001t0001g0150 a0001c0001t0002g0076 a0001c0001t0003g0002 others(59): Show |
63 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.972-1431A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858694 | |||||||
chr9:4858702 | A | C | 102 | a0001c0001t0001g0157 a0001c0001t0001g0255 a0001c0001t0001g0256 others(99): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.972-1423A>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858702 | |||||||
chr9:4858735 | C | A | 2 | a0001c0001t0008g0202 a0001c0001t0008g0203 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.972-1390C>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858735 | |||||||
chr9:4858746 | C | T | 3 | a0001c0001t0003g0119 a0001c0001t0003g0137 a0001c0001t0003g0139 |
3 | NA18956.hp1 NA19010.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.972-1379C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858746 | |||||||
chr9:4858749 | GA | G | 227 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.972-1375delA | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858749 | |||||||
chr9:4858806 | C | T | 27 | a0001c0001t0001g0174 a0001c0001t0001g0214 a0001c0001t0001g0306 others(24): Show |
27 | HG00741.hp2 HG01099.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.972-1319C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858806 | |||||||
chr9:4858861 | T | C | 4 | a0001c0001t0001g0347 a0001c0001t0002g0095 a0001c0001t0002g0349 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-1264T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858861 | |||||||
chr9:4858901 | G | A | 1 | a0001c0001t0005g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.972-1224G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858901 | |||||||
chr9:4858997 | G | A | 196 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.972-1128G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4858997 | |||||||
chr9:4859015 | A | G | 51 | a0001c0001t0001g0161 a0001c0001t0001g0174 a0001c0001t0001g0214 others(48): Show |
52 | HG00621.hp1 HG00741.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.972-1110A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859015 | |||||||
chr9:4859106 | T | C | 121 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0141 others(118): Show |
123 | HG00621.hp1 HG00735.hp2 HG00741.hp1 others(120): Show |
intron_variant | MODIFIER | c.972-1019T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859106 | |||||||
chr9:4859118 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.972-1007C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859118 | |||||||
chr9:4859252 | G | A | 5 | a0001c0001t0009g0003 a0001c0001t0009g0094 a0001c0001t0009g0101 others(2): Show |
6 | NA18939.hp2 NA18942.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-873G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859252 | |||||||
chr9:4859303 | A | G | 117 | a0001c0001t0001g0116 a0001c0001t0001g0134 a0001c0001t0001g0157 others(114): Show |
118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.972-822A>G | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859303 | |||||||
chr9:4859522 | G | T | 1 | a0001c0001t0003g0054 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.972-603G>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859522 | |||||||
chr9:4859569 | G | A | 1 | a0001c0001t0018g0312 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.972-556G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859569 | |||||||
chr9:4859621 | G | A | 1 | a0001c0001t0003g0377 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.972-504G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859621 | |||||||
chr9:4859692 | T | C | 4 | a0001c0001t0014g0194 a0001c0001t0014g0195 a0001c0001t0014g0368 others(1): Show |
4 | HG01981.hp1 HG02258.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.972-433T>C | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859692 | |||||||
chr9:4859872 | G | A | 23 | a0001c0001t0001g0310 a0001c0001t0003g0345 a0001c0001t0005g0293 others(20): Show |
23 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.972-253G>A | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859872 | |||||||
chr9:4859997 | C | T | 2 | a0001c0001t0021g0183 a0001c0001t0029g0140 |
2 | HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.972-128C>T | RCL1 | ENSG00000120158.12 | transcript | ENST00000381750.9 | protein_coding | 8/8 | chr9 | 4859997 |