Item | Value |
---|---|
geneid | 3746 |
ensemblid | ENSG00000129159.9 |
hgncid | 6233 |
symbol | KCNC1 |
name | potassium voltage-gated channel subfamily C member 1 |
refseq_nuc | NM_001112741.2 |
refseq_prot | NP_001106212.1 |
ensembl_nuc | ENST00000265969.8 |
ensembl_prot | ENSP00000265969.7 |
mane_status | MANE Select |
chr | chr11 |
start | 17734781 |
end | 17783057 |
strand | + |
ver | v1.2 |
region | chr11:17734781-17783057 |
region5000 | chr11:17729781-17788057 |
regionname0 | KCNC1_chr11_17734781_17783057 |
regionname5000 | KCNC1_chr11_17729781_17788057 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 585 | 331 | 95 | 60 | 116 | 18 | 40 | 74 | KCNC1_chr11_17729781_17788057 | KCNC1 | MGQGD others(580): Show |
chr11 | 17729781 | 17788057 |
a0002 | 0/0 | 585 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | MGQGD others(580): Show |
chr11 | 17729781 | 17788057 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1755 | 314 | 82 | 59 | 115 | 17 | 39 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0002 | 0/0 | 1755 | 7 | 7 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0003 | 0/0 | 1755 | 3 | 3 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0004 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0005 | 0/0 | 1755 | 2 | 0 | 1 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0006 | 0/0 | 1755 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0007 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0001c0008 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 | ||
a0002c0009 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | ATGGG others(1750): Show |
chr11 | 17729781 | 17788057 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4303 | 187 | 35 | 35 | 92 | 10 | 14 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0002 | 0/0 | 4303 | 35 | 7 | 5 | 11 | 1 | 11 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0003 | 0/0 | 4303 | 26 | 17 | 6 | 0 | 3 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0004 | 0/0 | 4303 | 11 | 3 | 1 | 0 | 0 | 7 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0005 | 0/0 | 4303 | 7 | 3 | 3 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0006 | 0/0 | 4303 | 5 | 0 | 4 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0007 | 0/0 | 4304 | 7 | 0 | 0 | 7 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4299): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0008 | 0/0 | 4303 | 5 | 3 | 0 | 0 | 2 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0009 | 0/0 | 4303 | 3 | 0 | 1 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0010 | 0/1 | 4303 | 2 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0011 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0012 | 0/0 | 4302 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4297): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0013 | 0/0 | 4303 | 2 | 0 | 0 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0014 | 0/0 | 4302 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4297): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0015 | 0/0 | 4303 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0016 | 0/0 | 4303 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0017 | 0/0 | 4303 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0018 | 0/0 | 4303 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0019 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0020 | 0/0 | 4303 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0021 | 0/0 | 4303 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0022 | 0/0 | 4303 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0023 | 0/0 | 4303 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0024 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0025 | 0/0 | 4302 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4297): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0026 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0027 | 0/0 | 4291 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4286): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0028 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0029 | 0/0 | 4291 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4286): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0030 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0031 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0032 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0001t0033 | 0/0 | 4303 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0002t0001 | 0/0 | 4303 | 4 | 4 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0002t0003 | 0/0 | 4303 | 3 | 3 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0003t0001 | 0/0 | 4303 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0003t0002 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0004t0003 | 0/0 | 4303 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0005t0006 | 0/0 | 4303 | 2 | 0 | 1 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0006t0005 | 0/0 | 4303 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0007t0011 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0001c0008t0001 | 0/0 | 4303 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
a0002c0009t0002 | 0/0 | 4303 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | GACCG others(4298): Show |
chr11 | 17729781 | 17788057 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0009g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0010g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0010g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0012g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0013g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0015g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0016g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0018g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0019g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0020g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0022g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0025g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0026g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0027g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0028g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0029g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0030g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0031g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0032g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0001t0033g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0004t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0004t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0005t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0005t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0006t0005g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0007t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0001c0008t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
a0002c0009t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0026 | EUR | GBR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0147 | EUR | GBR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00140 | hp1 | a0001 | c0005 | t0006 | g0133 | EUR | GBR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0078 | EUR | GBR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | FIN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00423 | hp2 | a0001 | c0001 | t0007 | g0074 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0104 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0132 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01069 | hp2 | a0001 | c0001 | t0015 | g0243 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0131 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01346 | hp2 | a0001 | c0001 | t0016 | g0195 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01361 | hp2 | a0001 | c0001 | t0009 | g0241 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0054 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0183 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01981 | hp2 | a0001 | c0001 | t0006 | g0126 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02080 | hp2 | a0001 | c0001 | t0020 | g0277 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02257 | hp1 | a0001 | c0001 | t0032 | g0065 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02258 | hp2 | a0001 | c0001 | t0031 | g0069 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0087 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02293 | hp2 | a0001 | c0001 | t0017 | g0196 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02300 | hp1 | a0001 | c0001 | t0010 | g0138 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0119 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02717 | hp1 | a0001 | c0001 | t0030 | g0095 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02717 | hp2 | a0001 | c0004 | t0003 | g0107 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02735 | hp2 | a0001 | c0001 | t0013 | g0164 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0030 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0020 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0303 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0016 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0064 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0111 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0015 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0015 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0250 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03579 | hp1 | a0001 | c0001 | t0026 | g0008 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03669 | hp2 | a0001 | c0006 | t0005 | g0101 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0134 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03704 | hp1 | a0001 | c0001 | t0023 | g0018 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03927 | hp1 | a0001 | c0001 | t0013 | g0144 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0016 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04228 | hp1 | a0001 | c0001 | t0022 | g0242 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | STU | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0300 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18941 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18952 | hp2 | a0001 | c0008 | t0001 | g0236 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18953 | hp2 | a0001 | c0001 | t0018 | g0169 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18968 | hp1 | a0001 | c0001 | t0033 | g0100 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18982 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18983 | hp2 | a0001 | c0001 | t0007 | g0084 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | LWK | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | LWK | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19085 | hp1 | a0001 | c0001 | t0029 | g0080 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19240 | hp1 | a0002 | c0009 | t0002 | g0097 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0108 | AFR | YRI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ASW | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20129 | hp2 | a0001 | c0001 | t0028 | g0305 | AFR | ASW | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20752 | hp1 | a0001 | c0001 | t0008 | g0025 | EUR | TSI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0240 | EUR | TSI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | GIH | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | GIH | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01123 | hp1 | a0001 | c0005 | t0006 | g0137 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02109 | hp2 | a0001 | c0007 | t0011 | g0211 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0109 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | ACB | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
HG06807 | hp2 | a0001 | c0001 | t0027 | g0304 | AFR | USA | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20300 | hp1 | a0001 | c0003 | t0002 | g0056 | AFR | USA | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | USA | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | LWK | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0130 | REF | REF | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0295 | REF | REF | KCNC1_chr11_17729781_17788057 | KCNC1 | chr11 | 17729781 | 17788057 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17771771 | A | T | 1 | a0002 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.677A>T | p.Asn226Ile | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 1899/4303 | 677/1758 | 226/585 | chr11 | 17771771 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17736074 | G | A | 2 | a0001c0002 a0001c0004 |
9 | HG01891.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
synonymous_variant | LOW | c.72G>A | p.Ser24Ser | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 1294/4303 | 72/1758 | 24/585 | chr11 | 17736074 | |||
chr11:17771838 | C | T | 1 | a0001c0005 | 2 | HG00140.hp1 HG01123.hp1 |
synonymous_variant | LOW | c.744C>T | p.Ile248Ile | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 1966/4303 | 744/1758 | 248/585 | chr11 | 17771838 | |||
chr11:17771844 | C | T | 1 | a0001c0008 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.750C>T | p.Gly250Gly | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 1972/4303 | 750/1758 | 250/585 | chr11 | 17771844 | |||
chr11:17772027 | C | T | 1 | a0001c0007 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.933C>T | p.Arg311Arg | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 2155/4303 | 933/1758 | 311/585 | chr11 | 17772027 | |||
chr11:17772111 | A | C | 1 | a0001c0003 | 3 | HG01891.hp1 HG02055.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1017A>C | p.Arg339Arg | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 2239/4303 | 1017/1758 | 339/585 | chr11 | 17772111 | |||
chr11:17772330 | C | T | 1 | a0001c0004 | 2 | HG02717.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.1236C>T | p.Ser412Ser | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/4 | 2458/4303 | 1236/1758 | 412/585 | chr11 | 17772330 | |||
chr11:17779613 | C | T | 1 | a0001c0006 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1662C>T | p.Tyr554Tyr | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/4 | 2884/4303 | 1662/1758 | 554/585 | chr11 | 17779613 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17734804 | G | T | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(11): Show |
61 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(58): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1199G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | chr11 | 17734804 | |||||||
chr11:17734807 | C | A | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0005t0006 |
8 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-1196C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 1196 | chr11 | 17734807 | ||||||
chr11:17734869 | G | A | 1 | a0001c0001t0015 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1134G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 1134 | chr11 | 17734869 | ||||||
chr11:17734917 | C | T | 1 | a0001c0001t0033 | 1 | NA18968.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1086C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | chr11 | 17734917 | |||||||
chr11:17734959 | C | G | 1 | a0001c0001t0026 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1044C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 1044 | chr11 | 17734959 | ||||||
chr11:17734970 | G | A | 2 | a0001c0001t0027 a0001c0001t0028 |
2 | HG06807.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-1033G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 1033 | chr11 | 17734970 | ||||||
chr11:17735149 | C | G | 1 | a0001c0001t0013 | 2 | HG02735.hp2 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-854C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 854 | chr11 | 17735149 | ||||||
chr11:17735241 | A | G | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0024 others(1): Show |
18 | HG00099.hp1 HG00738.hp2 HG02559.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-762A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 762 | chr11 | 17735241 | ||||||
chr11:17735314 | C | CG | 1 | a0001c0001t0007 | 7 | HG00423.hp2 NA18941.hp1 NA18970.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-683dupG | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 682 | INFO_REALIGN_3_PRIME | chr11 | 17735314 | |||||
chr11:17735520 | G | T | 1 | a0001c0001t0023 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-483G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 483 | chr11 | 17735520 | ||||||
chr11:17735684 | CCTCCCTC others(5): Show |
C | 2 | a0001c0001t0027 a0001c0001t0029 |
2 | HG06807.hp2 NA19085.hp1 |
5_prime_UTR_variant | MODIFIER | c.-295_-284delTCTCCC others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 284 | INFO_REALIGN_3_PRIME | chr11 | 17735684 | |||||
chr11:17735740 | C | G | 2 | a0001c0001t0009 a0001c0001t0022 |
4 | HG01361.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-263C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 263 | chr11 | 17735740 | ||||||
chr11:17735870 | C | A | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | HG01346.hp2 HG02293.hp2 |
5_prime_UTR_variant | MODIFIER | c.-133C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/4 | 133 | chr11 | 17735870 | ||||||
chr11:17781896 | CA | C | 3 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0025 |
5 | HG01884.hp1 HG02280.hp1 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*165delA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 165 | INFO_REALIGN_3_PRIME | chr11 | 17781896 | |||||
chr11:17781966 | A | T | 1 | a0001c0001t0021 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*232A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 232 | chr11 | 17781966 | ||||||
chr11:17782135 | G | A | 1 | a0001c0001t0018 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 401 | chr11 | 17782135 | ||||||
chr11:17782164 | A | G | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(15): Show |
64 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*430A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 430 | chr11 | 17782164 | ||||||
chr11:17782185 | G | A | 1 | a0001c0001t0030 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*451G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 451 | chr11 | 17782185 | ||||||
chr11:17782392 | C | T | 1 | a0001c0001t0020 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*658C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 658 | chr11 | 17782392 | ||||||
chr11:17782516 | C | T | 1 | a0001c0001t0022 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*782C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 782 | chr11 | 17782516 | ||||||
chr11:17782603 | G | A | 6 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0030 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*869G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 869 | chr11 | 17782603 | ||||||
chr11:17783011 | C | T | 1 | a0001c0001t0019 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1277C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 1277 | chr11 | 17783011 | ||||||
chr11:17783049 | T | G | 1 | a0001c0001t0031 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 4/4 | 1315 | chr11 | 17783049 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:17736664 | TA | T | 3 | a0001c0001t0005g0303 a0001c0001t0027g0304 a0001c0001t0028g0305 |
3 | HG02922.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.570+93delA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17736664 | |||||||
chr11:17736914 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.570+342T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17736914 | |||||||
chr11:17737039 | G | A | 1 | a0001c0001t0023g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.570+467G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737039 | |||||||
chr11:17737040 | T | C | 103 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.570+468T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737040 | |||||||
chr11:17737047 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.570+475G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737047 | |||||||
chr11:17737393 | G | A | 1 | a0001c0001t0005g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.570+821G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737393 | |||||||
chr11:17737649 | C | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(85): Show |
90 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.570+1077C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737649 | |||||||
chr11:17737658 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.570+1086G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737658 | |||||||
chr11:17737672 | G | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.570+1100G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737672 | |||||||
chr11:17737883 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.570+1311A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737883 | |||||||
chr11:17737906 | T | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(17): Show |
20 | HG00735.hp1 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.570+1334T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17737906 | |||||||
chr11:17737928 | TG | T | 59 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0034 others(56): Show |
61 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.570+1359delG | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17737928 | ||||||
chr11:17738007 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.570+1435C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738007 | |||||||
chr11:17738253 | C | G | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.570+1681C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738253 | |||||||
chr11:17738257 | C | G | 1 | a0001c0001t0015g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.570+1685C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738257 | |||||||
chr11:17738503 | A | C | 2 | a0001c0001t0005g0103 a0001c0001t0005g0104 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.570+1931A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738503 | |||||||
chr11:17738526 | A | C | 1 | a0001c0001t0001g0302 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.570+1954A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738526 | |||||||
chr11:17738542 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.570+1970G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738542 | |||||||
chr11:17738611 | C | T | 1 | a0001c0001t0014g0102 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.570+2039C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738611 | |||||||
chr11:17738713 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.570+2141G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17738713 | |||||||
chr11:17739035 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.570+2463C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739035 | |||||||
chr11:17739036 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.570+2464G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739036 | |||||||
chr11:17739048 | T | G | 1 | a0001c0001t0005g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.570+2476T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739048 | |||||||
chr11:17739077 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.570+2505T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739077 | |||||||
chr11:17739098 | C | T | 3 | a0001c0001t0009g0015 a0001c0001t0009g0241 a0001c0001t0022g0242 |
4 | HG01361.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+2526C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739098 | |||||||
chr11:17739127 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.570+2555T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739127 | |||||||
chr11:17739141 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.570+2569T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739141 | |||||||
chr11:17739199 | G | A | 9 | a0001c0002t0001g0106 a0001c0002t0001g0109 a0001c0002t0001g0110 others(6): Show |
9 | HG01891.hp2 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+2627G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739199 | |||||||
chr11:17739204 | T | G | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.570+2632T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739204 | |||||||
chr11:17739211 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.570+2639G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739211 | |||||||
chr11:17739330 | TGTG | T | 3 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0003g0240 |
3 | HG00735.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.570+2759_570+2761d others(5): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739330 | |||||||
chr11:17739357 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.570+2785C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739357 | |||||||
chr11:17739362 | C | CGT | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(10): Show |
13 | HG00735.hp1 HG01255.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+2826_570+2827d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | C | CGTGT | 3 | a0001c0001t0001g0049 a0001c0001t0002g0099 a0001c0001t0033g0100 |
3 | HG01515.hp1 HG02809.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.570+2824_570+2827d others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGT | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0002g0059 others(8): Show |
11 | HG01168.hp2 HG01891.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.570+2826_570+2827d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGT | C | 5 | a0001c0001t0001g0290 a0001c0001t0002g0057 a0001c0001t0002g0058 others(2): Show |
5 | HG02055.hp2 HG02723.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+2824_570+2827d others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0001g0237 a0001c0001t0001g0286 a0001c0001t0001g0287 others(23): Show |
27 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.570+2820_570+2827d others(10): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(3): Show |
C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
72 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.570+2818_570+2827d others(12): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0001g0212 a0001c0007t0011g0211 |
2 | HG02109.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.570+2816_570+2827d others(14): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(7): Show |
C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.570+2814_570+2827d others(16): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0023g0018 |
3 | HG03704.hp1 NA19012.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.570+2812_570+2827d others(18): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739362 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.570+2810_570+2827d others(20): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739362 | ||||||
chr11:17739612 | C | A | 1 | a0001c0001t0002g0063 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.570+3040C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739612 | |||||||
chr11:17739613 | G | A | 1 | a0001c0001t0005g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.570+3041G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739613 | |||||||
chr11:17739673 | C | CTG | 7 | a0001c0001t0001g0210 a0001c0001t0001g0235 a0001c0001t0001g0290 others(4): Show |
7 | HG00639.hp1 HG02083.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+3129_570+3130d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739673 | ||||||
chr11:17739673 | CTG | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.570+3129_570+3130d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739673 | ||||||
chr11:17739673 | CTGTG | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0036 others(37): Show |
41 | HG00408.hp2 HG00735.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.570+3127_570+3130d others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739673 | ||||||
chr11:17739673 | CTGTGTG | C | 53 | a0001c0001t0001g0286 a0001c0001t0002g0010 a0001c0001t0002g0053 others(50): Show |
55 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.570+3125_570+3130d others(8): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17739673 | ||||||
chr11:17739695 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.570+3123G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739695 | |||||||
chr11:17739709 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+3137G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739709 | |||||||
chr11:17739817 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.570+3245C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739817 | |||||||
chr11:17739968 | C | G | 5 | a0001c0001t0001g0218 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG00733.hp2 HG01168.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+3396C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739968 | |||||||
chr11:17739969 | G | A | 1 | a0001c0001t0005g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.570+3397G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17739969 | |||||||
chr11:17740086 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0234 |
2 | NA19005.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.570+3514C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740086 | |||||||
chr11:17740172 | G | A | 1 | a0001c0003t0002g0056 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.570+3600G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740172 | |||||||
chr11:17740201 | G | T | 3 | a0001c0001t0005g0303 a0001c0001t0027g0304 a0001c0001t0028g0305 |
3 | HG02922.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.570+3629G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740201 | |||||||
chr11:17740209 | T | A | 13 | a0001c0001t0001g0116 a0001c0001t0001g0139 a0001c0001t0001g0140 others(10): Show |
13 | HG01256.hp1 HG01496.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.570+3637T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740209 | |||||||
chr11:17740310 | T | G | 1 | a0001c0001t0005g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.570+3738T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740310 | |||||||
chr11:17740315 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.570+3743A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740315 | |||||||
chr11:17740333 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.570+3761G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740333 | |||||||
chr11:17740546 | T | G | 15 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0292 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.570+3974T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740546 | |||||||
chr11:17740661 | T | C | 3 | a0001c0002t0001g0106 a0001c0004t0003g0107 a0001c0004t0003g0108 |
3 | HG02717.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.570+4089T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740661 | |||||||
chr11:17740952 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0290 others(3): Show |
6 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.570+4380G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17740952 | |||||||
chr11:17741025 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0142 a0001c0001t0001g0290 others(5): Show |
8 | HG01891.hp2 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+4453G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741025 | |||||||
chr11:17741160 | C | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+4588C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741160 | |||||||
chr11:17741227 | C | G | 1 | a0001c0001t0002g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+4655C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741227 | |||||||
chr11:17741250 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.570+4678A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741250 | |||||||
chr11:17741306 | G | T | 1 | a0001c0001t0003g0289 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.570+4734G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741306 | |||||||
chr11:17741315 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(28): Show |
31 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.570+4743G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741315 | |||||||
chr11:17741322 | C | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0246 a0001c0001t0003g0289 |
3 | HG00280.hp1 HG00639.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.570+4750C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741322 | |||||||
chr11:17741426 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0002g0096 a0001c0001t0030g0095 others(1): Show |
4 | HG02717.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+4854T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741426 | |||||||
chr11:17741487 | C | T | 1 | a0001c0001t0003g0289 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.570+4915C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741487 | |||||||
chr11:17741530 | T | A | 2 | a0001c0001t0003g0299 a0001c0001t0019g0300 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.570+4958T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741530 | |||||||
chr11:17741541 | C | T | 8 | a0001c0001t0001g0233 a0001c0001t0002g0061 a0001c0001t0002g0091 others(5): Show |
8 | HG02056.hp2 HG02922.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+4969C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741541 | |||||||
chr11:17741637 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.570+5065C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741637 | |||||||
chr11:17741692 | G | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG01255.hp1 HG01928.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+5120G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741692 | |||||||
chr11:17741876 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
8 | HG00558.hp1 NA18945.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+5304C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741876 | |||||||
chr11:17741898 | G | C | 7 | a0001c0001t0002g0066 a0001c0001t0004g0019 a0001c0001t0004g0032 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.570+5326G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741898 | |||||||
chr11:17741918 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.570+5346C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17741918 | |||||||
chr11:17742004 | C | G | 1 | a0002c0009t0002g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.570+5432C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17742004 | |||||||
chr11:17742130 | C | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | HG00735.hp2 HG01106.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+5558C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17742130 | |||||||
chr11:17742190 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.570+5618C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17742190 | |||||||
chr11:17742664 | A | T | 1 | a0001c0001t0001g0205 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.570+6092A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17742664 | |||||||
chr11:17743268 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0246 |
2 | HG00280.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.570+6696G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743268 | |||||||
chr11:17743283 | G | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(51): Show |
54 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.570+6711G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743283 | |||||||
chr11:17743366 | C | T | 48 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(45): Show |
48 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.570+6794C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743366 | |||||||
chr11:17743634 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.570+7062G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743634 | |||||||
chr11:17743723 | C | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
20 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.570+7151C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743723 | |||||||
chr11:17743788 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG02135.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.570+7216C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743788 | |||||||
chr11:17743840 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.570+7268T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743840 | |||||||
chr11:17743854 | C | T | 1 | a0001c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.570+7282C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743854 | |||||||
chr11:17743884 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG02965.hp1 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.570+7312G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743884 | |||||||
chr11:17743994 | C | T | 2 | a0001c0001t0001g0047 a0001c0002t0003g0105 |
2 | HG01255.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.570+7422C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17743994 | |||||||
chr11:17744022 | G | A | 8 | a0001c0001t0002g0066 a0001c0001t0003g0017 a0001c0001t0004g0019 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+7450G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744022 | |||||||
chr11:17744181 | G | A | 2 | a0001c0001t0002g0059 a0001c0001t0002g0067 |
2 | NA19070.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.570+7609G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744181 | |||||||
chr11:17744271 | A | G | 24 | a0001c0001t0001g0208 a0001c0001t0001g0233 a0001c0001t0001g0246 others(21): Show |
24 | HG00280.hp1 HG01257.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.570+7699A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744271 | |||||||
chr11:17744501 | T | C | 11 | a0001c0001t0001g0208 a0001c0001t0001g0246 a0001c0001t0002g0034 others(8): Show |
11 | HG00280.hp1 HG01257.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+7929T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744501 | |||||||
chr11:17744512 | G | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0246 |
2 | HG00280.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.570+7940G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744512 | |||||||
chr11:17744515 | CTGGGGGG others(4): Show |
C | 6 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+7944_570+7954d others(13): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744515 | |||||||
chr11:17744554 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+7982T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744554 | |||||||
chr11:17744571 | G | A | 2 | a0001c0001t0001g0047 a0001c0002t0003g0105 |
2 | HG01255.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.570+7999G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744571 | |||||||
chr11:17744632 | T | G | 6 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+8060T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744632 | |||||||
chr11:17744743 | A | G | 24 | a0001c0001t0001g0208 a0001c0001t0001g0233 a0001c0001t0001g0246 others(21): Show |
24 | HG00280.hp1 HG01257.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.570+8171A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744743 | |||||||
chr11:17744843 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.570+8271G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744843 | |||||||
chr11:17744844 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.570+8272G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17744844 | |||||||
chr11:17745079 | C | A | 8 | a0001c0001t0002g0066 a0001c0001t0003g0017 a0001c0001t0004g0019 others(5): Show |
8 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.570+8507C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745079 | |||||||
chr11:17745300 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.570+8728A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745300 | |||||||
chr11:17745414 | G | A | 3 | a0001c0001t0005g0303 a0001c0001t0027g0304 a0001c0001t0028g0305 |
3 | HG02922.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.570+8842G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745414 | |||||||
chr11:17745434 | C | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.570+8862C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745434 | |||||||
chr11:17745615 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0246 |
2 | HG00280.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.570+9043C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745615 | |||||||
chr11:17745762 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0206 |
4 | NA18967.hp1 NA18980.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+9190C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745762 | |||||||
chr11:17745767 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.570+9195C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745767 | |||||||
chr11:17745852 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.570+9280C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745852 | |||||||
chr11:17745855 | C | T | 4 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG02486.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+9283C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745855 | |||||||
chr11:17745979 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.570+9407T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17745979 | |||||||
chr11:17746014 | A | T | 1 | a0001c0001t0002g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.570+9442A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746014 | |||||||
chr11:17746108 | G | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.570+9536G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746108 | |||||||
chr11:17746402 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.570+9830A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746402 | |||||||
chr11:17746447 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.570+9875G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746447 | |||||||
chr11:17746515 | C | T | 1 | a0001c0001t0003g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+9943C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746515 | |||||||
chr11:17746532 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.570+9960C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746532 | |||||||
chr11:17746778 | C | T | 6 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(3): Show |
7 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+10206C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746778 | |||||||
chr11:17746998 | T | C | 9 | a0001c0001t0002g0034 a0001c0001t0002g0066 a0001c0001t0003g0017 others(6): Show |
9 | HG02257.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+10426T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17746998 | |||||||
chr11:17747112 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.570+10540C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747112 | |||||||
chr11:17747114 | G | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.570+10542G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747114 | |||||||
chr11:17747145 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(47): Show |
54 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.570+10573C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747145 | |||||||
chr11:17747180 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+10608G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747180 | |||||||
chr11:17747356 | G | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.570+10784G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747356 | |||||||
chr11:17747518 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.570+10946G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747518 | |||||||
chr11:17747585 | C | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
35 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.570+11013C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747585 | |||||||
chr11:17747614 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.570+11042G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747614 | |||||||
chr11:17747671 | C | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(51): Show |
58 | HG00558.hp1 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.570+11099C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747671 | |||||||
chr11:17747706 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.570+11134G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747706 | |||||||
chr11:17747786 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.570+11214G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747786 | |||||||
chr11:17747838 | C | A | 1 | a0001c0001t0009g0015 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.570+11266C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747838 | |||||||
chr11:17747848 | G | T | 3 | a0001c0001t0001g0197 a0001c0001t0003g0216 a0001c0001t0005g0104 |
3 | HG00323.hp1 HG00733.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.570+11276G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747848 | |||||||
chr11:17747932 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.570+11360C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17747932 | |||||||
chr11:17748185 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.570+11613G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748185 | |||||||
chr11:17748208 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.570+11636G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748208 | |||||||
chr11:17748242 | A | G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(39): Show |
42 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.570+11670A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748242 | |||||||
chr11:17748261 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
10 | HG00544.hp1 HG01981.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.570+11689A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748261 | |||||||
chr11:17748262 | C | T | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.570+11690C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748262 | |||||||
chr11:17748331 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.570+11759C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748331 | |||||||
chr11:17748371 | A | G | 6 | a0001c0001t0005g0303 a0001c0001t0027g0304 a0001c0001t0028g0305 others(3): Show |
6 | HG01891.hp1 HG02055.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.570+11799A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748371 | |||||||
chr11:17748706 | C | T | 14 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0001g0225 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.570+12134C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748706 | |||||||
chr11:17748719 | A | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+12147A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748719 | |||||||
chr11:17748844 | C | T | 1 | a0001c0001t0010g0138 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.570+12272C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17748844 | |||||||
chr11:17749004 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.570+12432T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749004 | |||||||
chr11:17749013 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.570+12441A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749013 | |||||||
chr11:17749052 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+12480G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749052 | |||||||
chr11:17749095 | C | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(83): Show |
90 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.570+12523C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749095 | |||||||
chr11:17749179 | C | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.570+12607C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749179 | |||||||
chr11:17749266 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.570+12694G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749266 | |||||||
chr11:17749267 | A | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
283 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.570+12695A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749267 | |||||||
chr11:17749286 | T | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(41): Show |
44 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.570+12714T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749286 | |||||||
chr11:17749364 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
283 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.570+12792A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749364 | |||||||
chr11:17749383 | A | C | 3 | a0001c0001t0005g0303 a0001c0001t0027g0304 a0001c0001t0028g0305 |
3 | HG02922.hp2 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.570+12811A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749383 | |||||||
chr11:17749401 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.570+12829A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749401 | |||||||
chr11:17749441 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(70): Show |
77 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.570+12869A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749441 | |||||||
chr11:17749557 | A | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.570+12985A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749557 | |||||||
chr11:17749574 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.570+13002G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749574 | |||||||
chr11:17749621 | G | A | 45 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(42): Show |
45 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.570+13049G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749621 | |||||||
chr11:17749638 | G | A | 7 | a0001c0001t0001g0190 a0001c0001t0003g0014 a0001c0001t0003g0050 others(4): Show |
8 | HG01884.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.570+13066G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749638 | |||||||
chr11:17749643 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.570+13071C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749643 | |||||||
chr11:17749655 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.570+13083C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749655 | |||||||
chr11:17749770 | C | T | 3 | a0001c0003t0001g0035 a0001c0003t0001g0118 a0001c0003t0002g0056 |
3 | HG01891.hp1 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.570+13198C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749770 | |||||||
chr11:17749814 | A | T | 9 | a0001c0001t0001g0245 a0001c0001t0002g0034 a0001c0001t0002g0066 others(6): Show |
9 | HG02145.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+13242A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749814 | |||||||
chr11:17749866 | A | G | 2 | a0001c0001t0027g0304 a0001c0001t0028g0305 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.570+13294A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749866 | |||||||
chr11:17749887 | C | T | 9 | a0001c0001t0001g0047 a0001c0001t0001g0233 a0001c0001t0002g0091 others(6): Show |
9 | HG01255.hp2 HG02056.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.570+13315C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749887 | |||||||
chr11:17749940 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
291 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.570+13368C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17749940 | |||||||
chr11:17750013 | T | C | 46 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(43): Show |
46 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.570+13441T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750013 | |||||||
chr11:17750077 | G | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.570+13505G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750077 | |||||||
chr11:17750088 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0015g0243 |
2 | HG01069.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.570+13516G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750088 | |||||||
chr11:17750343 | C | A | 1 | a0001c0007t0011g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.570+13771C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750343 | |||||||
chr11:17750547 | G | C | 1 | a0001c0001t0003g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.570+13975G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750547 | |||||||
chr11:17750627 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+14055G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750627 | |||||||
chr11:17750630 | C | G | 4 | a0001c0001t0001g0301 a0001c0001t0003g0129 a0001c0001t0005g0077 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+14058C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750630 | |||||||
chr11:17750680 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.570+14108G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750680 | |||||||
chr11:17750718 | G | A | 4 | a0001c0001t0001g0301 a0001c0001t0003g0129 a0001c0001t0005g0077 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+14146G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750718 | |||||||
chr11:17750820 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(22): Show |
25 | HG00735.hp1 HG01070.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.570+14248C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750820 | |||||||
chr11:17750923 | A | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(83): Show |
90 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.570+14351A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17750923 | |||||||
chr11:17751033 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(44): Show |
51 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.570+14461G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751033 | |||||||
chr11:17751067 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.570+14495A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751067 | |||||||
chr11:17751193 | G | A | 1 | a0001c0001t0031g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.570+14621G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751193 | |||||||
chr11:17751198 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.570+14626A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751198 | |||||||
chr11:17751223 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.570+14651G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751223 | |||||||
chr11:17751266 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+14694C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751266 | |||||||
chr11:17751298 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.570+14726G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751298 | |||||||
chr11:17751309 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+14737G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751309 | |||||||
chr11:17751565 | G | A | 1 | a0001c0001t0004g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.570+14993G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751565 | |||||||
chr11:17751732 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0003g0217 |
2 | HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.570+15160G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751732 | |||||||
chr11:17751779 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(92): Show |
99 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.570+15207A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751779 | |||||||
chr11:17751872 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.570+15300A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17751872 | |||||||
chr11:17752039 | G | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(45): Show |
52 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.570+15467G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752039 | |||||||
chr11:17752170 | C | G | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+15598C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752170 | |||||||
chr11:17752193 | C | G | 2 | a0001c0001t0004g0022 a0001c0001t0004g0030 |
2 | HG02683.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.570+15621C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752193 | |||||||
chr11:17752480 | T | C | 9 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(6): Show |
9 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+15908T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752480 | |||||||
chr11:17752488 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
277 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.570+15916T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752488 | |||||||
chr11:17752489 | G | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(46): Show |
53 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.570+15917G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752489 | |||||||
chr11:17752658 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.570+16086A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752658 | |||||||
chr11:17752681 | T | C | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.570+16109T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752681 | |||||||
chr11:17752740 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.570+16168T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752740 | |||||||
chr11:17752926 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.570+16354A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17752926 | |||||||
chr11:17753023 | G | T | 3 | a0001c0001t0004g0019 a0001c0001t0008g0021 a0001c0002t0001g0106 |
3 | HG02615.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.570+16451G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753023 | |||||||
chr11:17753187 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0200 a0001c0001t0003g0002 |
5 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+16615G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753187 | |||||||
chr11:17753247 | T | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(84): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.570+16675T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753247 | |||||||
chr11:17753259 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.570+16687G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753259 | |||||||
chr11:17753276 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.570+16704C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753276 | |||||||
chr11:17753482 | G | A | 87 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(84): Show |
91 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.570+16910G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753482 | |||||||
chr11:17753629 | G | A | 1 | a0001c0007t0011g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.570+17057G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753629 | |||||||
chr11:17753695 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.570+17123C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753695 | |||||||
chr11:17753850 | C | T | 1 | a0001c0005t0006g0137 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.570+17278C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753850 | |||||||
chr11:17753900 | G | C | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.570+17328G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17753900 | |||||||
chr11:17754192 | C | A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(83): Show |
90 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.571-17473C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754192 | |||||||
chr11:17754252 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(45): Show |
52 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.571-17413G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754252 | |||||||
chr11:17754272 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.571-17393G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754272 | |||||||
chr11:17754492 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.571-17173C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754492 | |||||||
chr11:17754495 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571-17170C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754495 | |||||||
chr11:17754561 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.571-17104G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754561 | |||||||
chr11:17754566 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-17099G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754566 | |||||||
chr11:17754568 | A | C | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17097A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754568 | |||||||
chr11:17754570 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17095G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754570 | |||||||
chr11:17754571 | T | A | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17094T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754571 | |||||||
chr11:17754578 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17087A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754578 | |||||||
chr11:17754581 | A | T | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17084A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754581 | |||||||
chr11:17754584 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-17081C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754584 | |||||||
chr11:17754585 | A | G | 10 | a0001c0001t0001g0233 a0001c0001t0002g0091 a0001c0001t0002g0092 others(7): Show |
10 | HG01884.hp1 HG02056.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-17080A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754585 | |||||||
chr11:17754592 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.571-17073C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754592 | |||||||
chr11:17754631 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.571-17034C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754631 | |||||||
chr11:17754632 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.571-17033C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17754632 | |||||||
chr11:17754667 | AGTTGGAG others(1): Show |
A | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-16994_571-1698 others(12): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17754667 | ||||||
chr11:17755116 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0002g0088 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.571-16549G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755116 | |||||||
chr11:17755203 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.571-16462G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755203 | |||||||
chr11:17755218 | T | A | 1 | a0001c0001t0003g0289 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.571-16447T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755218 | |||||||
chr11:17755330 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-16335G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755330 | |||||||
chr11:17755354 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(35): Show |
38 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.571-16311A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755354 | |||||||
chr11:17755425 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.571-16240C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755425 | |||||||
chr11:17755554 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-16111C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17755554 | |||||||
chr11:17756322 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-15343T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756322 | |||||||
chr11:17756323 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-15342A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756323 | |||||||
chr11:17756326 | T | C | 1 | a0001c0002t0003g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.571-15339T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756326 | |||||||
chr11:17756384 | C | A | 1 | a0001c0001t0008g0025 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.571-15281C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756384 | |||||||
chr11:17756520 | A | AAC | 10 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0233 others(7): Show |
10 | HG01069.hp2 HG01884.hp1 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-15108_571-1510 others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | A | AACAC | 5 | a0001c0001t0001g0257 a0001c0001t0002g0093 a0001c0001t0003g0017 others(2): Show |
5 | HG01074.hp1 HG01358.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-15110_571-1510 others(8): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | A | AACACAC | 7 | a0001c0001t0001g0145 a0001c0001t0001g0208 a0001c0001t0001g0218 others(4): Show |
7 | HG00280.hp1 HG00733.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-15112_571-1510 others(10): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | AAC | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(88): Show |
96 | HG00558.hp1 HG00639.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.571-15108_571-1510 others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | AACAC | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0047 others(45): Show |
52 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.571-15110_571-1510 others(8): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | AACACAC | A | 9 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0079 others(6): Show |
9 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-15112_571-1510 others(10): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | AACACACA others(1): Show |
A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(98): Show |
113 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.571-15114_571-1510 others(12): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756520 | AACACACA others(7): Show |
A | 1 | a0001c0002t0003g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.571-15120_571-1510 others(18): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17756520 | ||||||
chr11:17756546 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.571-15119C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756546 | |||||||
chr11:17756615 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.571-15050G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756615 | |||||||
chr11:17756666 | A | G | 1 | a0001c0001t0007g0086 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.571-14999A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756666 | |||||||
chr11:17756693 | T | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0290 a0001c0002t0001g0109 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-14972T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756693 | |||||||
chr11:17756959 | C | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
294 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.571-14706C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756959 | |||||||
chr11:17756983 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.571-14682G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17756983 | |||||||
chr11:17757011 | TAATCTGC others(2): Show |
T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0135 a0001c0001t0001g0136 others(13): Show |
18 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-14650_571-1464 others(13): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17757011 | ||||||
chr11:17757042 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0161 a0001c0001t0001g0182 others(1): Show |
4 | NA18967.hp2 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-14623T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757042 | |||||||
chr11:17757050 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
294 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.571-14615G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757050 | |||||||
chr11:17757145 | A | G | 5 | a0001c0001t0001g0233 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | HG02056.hp2 HG03195.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-14520A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757145 | |||||||
chr11:17757213 | GCCA | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-14450_571-1444 others(7): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17757213 | ||||||
chr11:17757240 | G | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0290 a0001c0002t0001g0109 others(2): Show |
5 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-14425G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757240 | |||||||
chr11:17757297 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.571-14368C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757297 | |||||||
chr11:17757315 | A | C | 1 | a0001c0001t0031g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-14350A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757315 | |||||||
chr11:17757316 | G | T | 1 | a0001c0001t0031g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-14349G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757316 | |||||||
chr11:17757320 | G | C | 10 | a0001c0001t0001g0233 a0001c0001t0002g0091 a0001c0001t0002g0092 others(7): Show |
10 | HG01884.hp1 HG02056.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.571-14345G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757320 | |||||||
chr11:17757545 | A | G | 1 | a0001c0001t0003g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.571-14120A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17757545 | |||||||
chr11:17758107 | A | T | 1 | a0001c0004t0003g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.571-13558A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758107 | |||||||
chr11:17758281 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-13384C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758281 | |||||||
chr11:17758304 | G | A | 5 | a0001c0001t0001g0233 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | HG02056.hp2 HG03195.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-13361G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758304 | |||||||
chr11:17758404 | A | C | 1 | a0001c0001t0002g0099 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.571-13261A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758404 | |||||||
chr11:17758426 | C | T | 1 | a0001c0001t0019g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.571-13239C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758426 | |||||||
chr11:17758726 | T | G | 1 | a0001c0001t0001g0235 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.571-12939T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758726 | |||||||
chr11:17758801 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-12864C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17758801 | |||||||
chr11:17759032 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(93): Show |
100 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.571-12633G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759032 | |||||||
chr11:17759277 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0123 a0001c0001t0001g0155 others(2): Show |
5 | HG00408.hp2 HG01928.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-12388G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759277 | |||||||
chr11:17759336 | T | C | 1 | a0001c0001t0003g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-12329T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759336 | |||||||
chr11:17759577 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-12088C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759577 | |||||||
chr11:17759608 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(35): Show |
38 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.571-12057G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759608 | |||||||
chr11:17759675 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-11990G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759675 | |||||||
chr11:17759877 | A | T | 1 | a0001c0002t0001g0110 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.571-11788A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17759877 | |||||||
chr11:17760061 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.571-11604C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760061 | |||||||
chr11:17760137 | G | GA | 38 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(35): Show |
38 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.571-11522dupA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17760137 | ||||||
chr11:17760305 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.571-11360C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760305 | |||||||
chr11:17760472 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-11193T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760472 | |||||||
chr11:17760482 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-11183G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760482 | |||||||
chr11:17760574 | A | C | 1 | a0001c0001t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.571-11091A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760574 | |||||||
chr11:17760650 | A | G | 7 | a0001c0001t0002g0066 a0001c0001t0004g0019 a0001c0001t0008g0021 others(4): Show |
7 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-11015A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760650 | |||||||
chr11:17760820 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-10845C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17760820 | |||||||
chr11:17761054 | G | A | 2 | a0001c0001t0002g0066 a0001c0001t0032g0065 |
2 | HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.571-10611G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761054 | |||||||
chr11:17761121 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-10544T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761121 | |||||||
chr11:17761272 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.571-10393G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761272 | |||||||
chr11:17761554 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-10111C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761554 | |||||||
chr11:17761566 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
184 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.571-10099G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761566 | |||||||
chr11:17761577 | A | T | 5 | a0001c0001t0001g0152 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
5 | HG00323.hp2 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-10088A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761577 | |||||||
chr11:17761742 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-9923A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761742 | |||||||
chr11:17761907 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA18959.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.571-9758A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761907 | |||||||
chr11:17761964 | A | G | 26 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(23): Show |
26 | HG00735.hp1 HG01070.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.571-9701A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761964 | |||||||
chr11:17761998 | C | A | 1 | a0001c0001t0004g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571-9667C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17761998 | |||||||
chr11:17762008 | G | T | 1 | a0001c0001t0004g0032 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.571-9657G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762008 | |||||||
chr11:17762015 | C | T | 3 | a0001c0001t0005g0303 a0001c0001t0012g0183 a0001c0001t0028g0305 |
3 | HG01884.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.571-9650C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762015 | |||||||
chr11:17762110 | C | A | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.571-9555C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762110 | |||||||
chr11:17762147 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-9518G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762147 | |||||||
chr11:17762148 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-9517G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762148 | |||||||
chr11:17762347 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.571-9318C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762347 | |||||||
chr11:17762756 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.571-8909T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762756 | |||||||
chr11:17762851 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0301 a0001c0001t0005g0077 others(1): Show |
4 | HG01255.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-8814A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762851 | |||||||
chr11:17762926 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.571-8739G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17762926 | |||||||
chr11:17763033 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0002g0033 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.571-8632T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763033 | |||||||
chr11:17763034 | A | G | 15 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0292 others(12): Show |
15 | HG01257.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.571-8631A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763034 | |||||||
chr11:17763049 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(8): Show |
11 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-8616C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763049 | |||||||
chr11:17763079 | G | A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571-8586G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763079 | |||||||
chr11:17763160 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(170): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.571-8505G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763160 | |||||||
chr11:17763397 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-8268G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763397 | |||||||
chr11:17763490 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.571-8175G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763490 | |||||||
chr11:17763564 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.571-8101C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763564 | |||||||
chr11:17763571 | T | TAC | 40 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(37): Show |
40 | HG00735.hp1 HG01070.hp1 HG02056.hp2 others(37): Show |
intron_variant | MODIFIER | c.571-8078_571-8077d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763571 | ||||||
chr11:17763571 | TAC | T | 4 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0004t0003g0107 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-8078_571-8077d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763571 | ||||||
chr11:17763636 | A | AC | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.571-8028dupC | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763636 | ||||||
chr11:17763638 | A | AC | 69 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0036 others(66): Show |
73 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.571-8022dupC | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763638 | ||||||
chr11:17763638 | A | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
217 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.571-8027A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763638 | |||||||
chr11:17763642 | C | CA | 5 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0139 others(2): Show |
5 | HG01256.hp1 HG01496.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-8023_571-8022i others(3): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763642 | |||||||
chr11:17763713 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.571-7952C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763713 | |||||||
chr11:17763716 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-7949C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763716 | |||||||
chr11:17763844 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-7821T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763844 | |||||||
chr11:17763886 | C | A | 1 | a0001c0007t0011g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.571-7779C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763886 | |||||||
chr11:17763908 | A | ACAC | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.571-7756_571-7754d others(5): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763908 | ||||||
chr11:17763949 | A | ACC | 58 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(55): Show |
62 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.571-7714_571-7713d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17763949 | ||||||
chr11:17763949 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
243 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.571-7716A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17763949 | |||||||
chr11:17764049 | AC | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0225 a0001c0001t0001g0279 others(3): Show |
9 | HG00544.hp1 HG02293.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-7611delC | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17764049 | ||||||
chr11:17764057 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-7608A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764057 | |||||||
chr11:17764137 | C | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0067 a0001c0001t0003g0289 others(1): Show |
4 | HG00639.hp1 HG02258.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-7528C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764137 | |||||||
chr11:17764251 | ACACACAC others(31): Show |
A | 29 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(26): Show |
29 | HG00735.hp1 HG01070.hp1 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.571-7401_571-7364d others(40): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17764251 | ||||||
chr11:17764265 | G | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(54): Show |
61 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.571-7400G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764265 | |||||||
chr11:17764271 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-7394A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764271 | |||||||
chr11:17764289 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-7376T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764289 | |||||||
chr11:17764370 | A | G | 1 | a0001c0001t0007g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.571-7295A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764370 | |||||||
chr11:17764435 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.571-7230C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764435 | |||||||
chr11:17764719 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0006g0126 |
2 | HG01175.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.571-6946T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764719 | |||||||
chr11:17764828 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0280 a0001c0001t0001g0282 |
6 | HG00544.hp1 HG02293.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-6837C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764828 | |||||||
chr11:17764829 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0005g0078 |
3 | HG00140.hp2 HG03017.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.571-6836G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764829 | |||||||
chr11:17764873 | A | G | 1 | a0001c0001t0003g0240 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.571-6792A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17764873 | |||||||
chr11:17765162 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.571-6503C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765162 | |||||||
chr11:17765298 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-6367C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765298 | |||||||
chr11:17765299 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-6366C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765299 | |||||||
chr11:17765304 | C | A | 1 | a0001c0001t0013g0164 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.571-6361C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765304 | |||||||
chr11:17765620 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.571-6045G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765620 | |||||||
chr11:17765626 | G | C | 12 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(9): Show |
12 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.571-6039G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765626 | |||||||
chr11:17765631 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-6034A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765631 | |||||||
chr11:17765632 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-6033G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765632 | |||||||
chr11:17765654 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-6011T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765654 | |||||||
chr11:17765668 | G | T | 1 | a0001c0001t0001g0177 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.571-5997G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765668 | |||||||
chr11:17765763 | G | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(29): Show |
32 | HG00735.hp1 HG01070.hp1 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.571-5902G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765763 | |||||||
chr11:17765794 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-5871G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765794 | |||||||
chr11:17765869 | C | G | 1 | a0001c0001t0001g0278 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.571-5796C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765869 | |||||||
chr11:17765952 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0257 a0001c0001t0003g0217 |
3 | HG01074.hp1 HG01358.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.571-5713C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765952 | |||||||
chr11:17765975 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-5690A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765975 | |||||||
chr11:17765982 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.571-5683G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17765982 | |||||||
chr11:17766091 | G | A | 2 | a0001c0001t0002g0063 a0001c0001t0013g0144 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.571-5574G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766091 | |||||||
chr11:17766243 | T | C | 4 | a0001c0001t0001g0246 a0001c0004t0003g0107 a0001c0004t0003g0108 others(1): Show |
4 | HG01257.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5422T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766243 | |||||||
chr11:17766248 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.571-5417C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766248 | |||||||
chr11:17766483 | C | G | 1 | a0001c0001t0002g0099 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.571-5182C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766483 | |||||||
chr11:17766608 | T | C | 4 | a0001c0001t0001g0246 a0001c0004t0003g0107 a0001c0004t0003g0108 others(1): Show |
4 | HG01257.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-5057T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766608 | |||||||
chr11:17766614 | T | C | 4 | a0001c0001t0002g0070 a0001c0001t0002g0082 a0001c0001t0008g0025 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-5051T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766614 | |||||||
chr11:17766728 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.571-4937C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766728 | |||||||
chr11:17766778 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.571-4887A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766778 | |||||||
chr11:17766853 | T | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
35 | HG00735.hp1 HG01070.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.571-4812T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766853 | |||||||
chr11:17766911 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
197 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.571-4754G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766911 | |||||||
chr11:17766964 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-4701T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766964 | |||||||
chr11:17766965 | A | C | 1 | a0001c0001t0002g0067 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-4700A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766965 | |||||||
chr11:17766966 | C | A | 1 | a0001c0001t0002g0067 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-4699C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766966 | |||||||
chr11:17766967 | C | A | 1 | a0001c0001t0002g0067 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.571-4698C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766967 | |||||||
chr11:17766967 | C | CA | 38 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0048 others(35): Show |
38 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.571-4681dupA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17766967 | ||||||
chr11:17766967 | C | CAA | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
261 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.571-4682_571-4681d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17766967 | ||||||
chr11:17766988 | G | T | 1 | a0001c0001t0005g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.571-4677G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17766988 | |||||||
chr11:17767131 | TA | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.571-4519delA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767131 | ||||||
chr11:17767137 | A | G | 44 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0139 others(41): Show |
48 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.571-4528A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767137 | |||||||
chr11:17767148 | T | C | 9 | a0001c0001t0002g0034 a0001c0001t0002g0066 a0001c0001t0004g0019 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-4517T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767148 | |||||||
chr11:17767152 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.571-4513C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767152 | |||||||
chr11:17767210 | G | A | 31 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(28): Show |
31 | HG00735.hp1 HG01070.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.571-4455G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767210 | |||||||
chr11:17767261 | T | C | 4 | a0001c0001t0001g0246 a0001c0004t0003g0107 a0001c0004t0003g0108 others(1): Show |
4 | HG01257.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-4404T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767261 | |||||||
chr11:17767284 | CA | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.571-4365delA | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767284 | ||||||
chr11:17767284 | CAAAAA | C | 7 | a0001c0001t0001g0197 a0001c0001t0003g0216 a0001c0001t0003g0219 others(4): Show |
7 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.571-4369_571-4365d others(7): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767284 | ||||||
chr11:17767291 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571-4369_571-4360d others(12): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767291 | ||||||
chr11:17767295 | AAAAAAGA others(4): Show |
A | 9 | a0001c0001t0002g0034 a0001c0001t0003g0046 a0001c0001t0004g0019 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-4365_571-4355d others(13): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767295 | ||||||
chr11:17767296 | A | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0139 others(29): Show |
36 | HG00558.hp1 HG00639.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.571-4369A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767296 | |||||||
chr11:17767296 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.571-4350_571-4341d others(12): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17767296 | ||||||
chr11:17767297 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.571-4368A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767297 | |||||||
chr11:17767402 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.571-4263T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767402 | |||||||
chr11:17767659 | G | A | 13 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(10): Show |
13 | HG00280.hp1 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.571-4006G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767659 | |||||||
chr11:17767743 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571-3922C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767743 | |||||||
chr11:17767763 | T | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.571-3902T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17767763 | |||||||
chr11:17768080 | C | T | 1 | a0001c0001t0004g0016 | 2 | HG03017.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.571-3585C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768080 | |||||||
chr11:17768087 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.571-3578T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768087 | |||||||
chr11:17768149 | C | T | 2 | a0001c0001t0005g0303 a0001c0001t0028g0305 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.571-3516C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768149 | |||||||
chr11:17768295 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.571-3370G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768295 | |||||||
chr11:17768299 | T | C | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571-3366T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768299 | |||||||
chr11:17768362 | C | T | 1 | a0001c0007t0011g0211 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.571-3303C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768362 | |||||||
chr11:17768612 | T | TG | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(75): Show |
85 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.571-3042dupG | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17768612 | ||||||
chr11:17768612 | T | TGG | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.571-3043_571-3042d others(4): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17768612 | ||||||
chr11:17768612 | T | TGGG | 18 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0136 others(15): Show |
18 | HG00140.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.571-3044_571-3042d others(5): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17768612 | ||||||
chr11:17768612 | TG | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(38): Show |
41 | HG01070.hp1 HG01256.hp1 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.571-3042delG | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr11 | 17768612 | ||||||
chr11:17768615 | G | C | 3 | a0001c0001t0001g0045 a0001c0001t0002g0092 a0001c0001t0013g0144 |
3 | HG00735.hp1 HG02056.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.571-3050G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768615 | |||||||
chr11:17768616 | G | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(29): Show |
32 | HG01070.hp1 HG01256.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.571-3049G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768616 | |||||||
chr11:17768622 | G | A | 4 | a0001c0001t0001g0246 a0001c0001t0004g0019 a0001c0001t0008g0021 others(1): Show |
4 | HG01257.hp2 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-3043G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768622 | |||||||
chr11:17768680 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.571-2985A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768680 | |||||||
chr11:17768895 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-2770C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768895 | |||||||
chr11:17768946 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.571-2719G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768946 | |||||||
chr11:17768997 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.571-2668C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768997 | |||||||
chr11:17768998 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0288 |
2 | HG01257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.571-2667G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17768998 | |||||||
chr11:17769162 | G | C | 1 | a0001c0001t0001g0261 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.571-2503G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769162 | |||||||
chr11:17769410 | A | G | 1 | a0001c0001t0031g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.571-2255A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769410 | |||||||
chr11:17769442 | G | A | 1 | a0001c0001t0003g0014 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.571-2223G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769442 | |||||||
chr11:17769621 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.571-2044T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769621 | |||||||
chr11:17769667 | C | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0264 |
2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.571-1998C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769667 | |||||||
chr11:17769698 | A | T | 6 | a0001c0001t0001g0189 a0001c0001t0001g0246 a0001c0001t0001g0291 others(3): Show |
6 | HG01257.hp2 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-1967A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769698 | |||||||
chr11:17769702 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.571-1963T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769702 | |||||||
chr11:17769820 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.571-1845A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769820 | |||||||
chr11:17769979 | T | C | 1 | a0001c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.571-1686T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769979 | |||||||
chr11:17769995 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.571-1670T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17769995 | |||||||
chr11:17770099 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.571-1566C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770099 | |||||||
chr11:17770170 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.571-1495C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770170 | |||||||
chr11:17770272 | G | C | 1 | a0001c0001t0002g0070 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.571-1393G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770272 | |||||||
chr11:17770275 | T | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0139 others(37): Show |
44 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.571-1390T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770275 | |||||||
chr11:17770384 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-1281G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770384 | |||||||
chr11:17770479 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.571-1186G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770479 | |||||||
chr11:17770498 | T | G | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571-1167T>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770498 | |||||||
chr11:17770545 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.571-1120G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770545 | |||||||
chr11:17770866 | G | A | 1 | a0001c0001t0005g0103 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.571-799G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770866 | |||||||
chr11:17770898 | C | T | 5 | a0001c0001t0001g0286 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG02451.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-767C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17770898 | |||||||
chr11:17771212 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.571-453C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771212 | |||||||
chr11:17771248 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.571-417A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771248 | |||||||
chr11:17771249 | G | GGTCACT | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.571-416_571-415ins others(6): Show |
KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771249 | |||||||
chr11:17771250 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.571-415C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771250 | |||||||
chr11:17771252 | A | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.571-413A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771252 | |||||||
chr11:17771254 | A | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.571-411A>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771254 | |||||||
chr11:17771260 | A | G | 1 | a0001c0001t0003g0299 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.571-405A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771260 | |||||||
chr11:17771443 | T | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(30): Show |
33 | HG00735.hp1 HG01070.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.571-222T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771443 | |||||||
chr11:17771493 | G | A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG02622.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571-172G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 1/3 | chr11 | 17771493 | |||||||
chr11:17772742 | G | A | 1 | a0001c0001t0008g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1504+144G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17772742 | |||||||
chr11:17772891 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0270 a0001c0001t0001g0272 others(3): Show |
6 | HG02083.hp2 HG02129.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1504+293A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17772891 | |||||||
chr11:17773046 | C | T | 1 | a0001c0001t0005g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1504+448C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773046 | |||||||
chr11:17773048 | G | A | 1 | a0001c0001t0015g0243 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1504+450G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773048 | |||||||
chr11:17773331 | G | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0145 a0001c0001t0001g0148 others(5): Show |
8 | HG00280.hp1 HG01069.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1504+733G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773331 | |||||||
chr11:17773358 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1504+760A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773358 | |||||||
chr11:17773477 | C | T | 1 | a0001c0004t0003g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1504+879C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773477 | |||||||
chr11:17773542 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0190 a0001c0001t0001g0194 others(20): Show |
27 | HG00558.hp1 HG01884.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.1504+944G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773542 | |||||||
chr11:17773597 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0270 a0001c0001t0001g0273 |
3 | HG02083.hp2 HG02129.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1504+999C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773597 | |||||||
chr11:17773880 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1504+1282C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17773880 | |||||||
chr11:17774182 | C | T | 54 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0122 others(51): Show |
54 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1504+1584C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774182 | |||||||
chr11:17774328 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1504+1730G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774328 | |||||||
chr11:17774379 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0012 others(113): Show |
119 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1504+1781C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774379 | |||||||
chr11:17774564 | A | C | 7 | a0001c0001t0001g0294 a0001c0001t0004g0019 a0001c0001t0008g0021 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1504+1966A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774564 | |||||||
chr11:17774705 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1504+2107T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774705 | |||||||
chr11:17774924 | G | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0172 a0001c0001t0001g0186 others(23): Show |
30 | HG00558.hp1 HG00673.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1504+2326G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774924 | |||||||
chr11:17774974 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1504+2376C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774974 | |||||||
chr11:17774991 | C | A | 35 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0047 others(32): Show |
35 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1504+2393C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774991 | |||||||
chr11:17774997 | A | G | 49 | a0001c0001t0001g0012 a0001c0001t0001g0045 a0001c0001t0001g0120 others(46): Show |
49 | HG00408.hp2 HG00423.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1504+2399A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17774997 | |||||||
chr11:17775020 | T | C | 3 | a0001c0001t0001g0246 a0001c0001t0001g0288 a0001c0001t0003g0017 |
3 | HG01257.hp2 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1504+2422T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775020 | |||||||
chr11:17775149 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1504+2551C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775149 | |||||||
chr11:17775354 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0005g0078 a0001c0001t0013g0144 |
4 | HG00140.hp2 HG03017.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1504+2756G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775354 | |||||||
chr11:17775602 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0228 a0001c0001t0001g0229 others(2): Show |
5 | HG00408.hp1 NA18950.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1504+3004A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775602 | |||||||
chr11:17775903 | G | T | 1 | a0001c0001t0003g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1504+3305G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775903 | |||||||
chr11:17775919 | C | T | 25 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(22): Show |
25 | HG00733.hp2 HG00735.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1504+3321C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775919 | |||||||
chr11:17775925 | C | G | 1 | a0001c0001t0003g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1504+3327C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17775925 | |||||||
chr11:17776125 | G | A | 1 | a0001c0001t0003g0249 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1505-3331G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776125 | |||||||
chr11:17776145 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0003g0017 |
2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1505-3311G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776145 | |||||||
chr11:17776162 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1505-3294T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776162 | |||||||
chr11:17776284 | C | G | 3 | a0001c0001t0001g0257 a0001c0001t0003g0217 a0001c0001t0015g0243 |
3 | HG01069.hp2 HG01074.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1505-3172C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776284 | |||||||
chr11:17776397 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0270 a0001c0001t0001g0273 |
3 | HG02083.hp2 HG02129.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1505-3059C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776397 | |||||||
chr11:17776419 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0271 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1505-3037G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776419 | |||||||
chr11:17776545 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1505-2911C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776545 | |||||||
chr11:17776638 | G | T | 1 | a0001c0001t0002g0094 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1505-2818G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776638 | |||||||
chr11:17776658 | G | A | 3 | a0001c0003t0001g0035 a0001c0003t0001g0118 a0001c0003t0002g0056 |
3 | HG01891.hp1 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1505-2798G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776658 | |||||||
chr11:17776718 | A | G | 13 | a0001c0001t0001g0197 a0001c0001t0003g0193 a0001c0001t0003g0216 others(10): Show |
13 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.1505-2738A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776718 | |||||||
chr11:17776807 | G | A | 2 | a0001c0004t0003g0107 a0001c0004t0003g0108 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1505-2649G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776807 | |||||||
chr11:17776908 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1505-2548G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17776908 | |||||||
chr11:17777011 | G | A | 1 | a0001c0001t0005g0303 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1505-2445G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777011 | |||||||
chr11:17777048 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1505-2408C>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777048 | |||||||
chr11:17777537 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1505-1919G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777537 | |||||||
chr11:17777542 | A | C | 1 | a0001c0001t0001g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1505-1914A>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777542 | |||||||
chr11:17777798 | C | T | 36 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0047 others(33): Show |
36 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.1505-1658C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777798 | |||||||
chr11:17777799 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1505-1657G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777799 | |||||||
chr11:17777897 | C | T | 14 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0003g0289 others(11): Show |
14 | HG00639.hp1 HG01496.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1505-1559C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777897 | |||||||
chr11:17777899 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1505-1557T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777899 | |||||||
chr11:17777926 | C | T | 2 | a0001c0001t0001g0279 a0001c0008t0001g0236 |
2 | NA18952.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1505-1530C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777926 | |||||||
chr11:17777957 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0245 a0001c0001t0002g0033 |
3 | HG02145.hp2 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1505-1499G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17777957 | |||||||
chr11:17778031 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1505-1425A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778031 | |||||||
chr11:17778032 | C | T | 5 | a0001c0001t0001g0152 a0001c0001t0001g0180 a0001c0001t0001g0202 others(2): Show |
5 | HG01123.hp2 HG01167.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1505-1424C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778032 | |||||||
chr11:17778039 | G | A | 1 | a0001c0001t0003g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1505-1417G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778039 | |||||||
chr11:17778127 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0136 a0001c0001t0002g0076 others(2): Show |
6 | HG00738.hp1 HG01175.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1505-1329C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778127 | |||||||
chr11:17778168 | T | A | 2 | a0001c0001t0001g0185 a0001c0001t0001g0260 |
2 | NA19060.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1505-1288T>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778168 | |||||||
chr11:17778174 | C | T | 2 | a0001c0001t0003g0299 a0001c0001t0004g0024 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1505-1282C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778174 | |||||||
chr11:17778789 | G | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
267 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.1505-667G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778789 | |||||||
chr11:17778869 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0232 |
2 | HG00544.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1505-587G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778869 | |||||||
chr11:17778969 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1505-487G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17778969 | |||||||
chr11:17779029 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
142 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1505-427G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17779029 | |||||||
chr11:17779234 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1505-222C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17779234 | |||||||
chr11:17779278 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1505-178C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17779278 | |||||||
chr11:17779362 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0002g0057 a0001c0001t0023g0018 |
3 | HG01361.hp1 HG03654.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1505-94G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17779362 | |||||||
chr11:17779376 | C | A | 53 | a0001c0001t0001g0038 a0001c0001t0001g0121 a0001c0001t0001g0124 others(50): Show |
54 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1505-80C>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 2/3 | chr11 | 17779376 | |||||||
chr11:17779673 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0122 a0001c0001t0001g0153 others(45): Show |
52 | HG00544.hp2 HG00558.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1693+29A>G | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17779673 | |||||||
chr11:17779735 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1693+91G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17779735 | |||||||
chr11:17779888 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1693+244G>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17779888 | |||||||
chr11:17780382 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1693+738G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780382 | |||||||
chr11:17780486 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1693+842G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780486 | |||||||
chr11:17780637 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1693+993T>C | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780637 | |||||||
chr11:17780763 | G | A | 1 | a0001c0006t0005g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1694-907G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780763 | |||||||
chr11:17780766 | C | T | 2 | a0001c0001t0001g0291 a0001c0002t0001g0113 |
2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1694-904C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780766 | |||||||
chr11:17780772 | C | T | 1 | a0001c0001t0003g0251 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1694-898C>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780772 | |||||||
chr11:17780807 | G | T | 1 | a0001c0001t0008g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1694-863G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780807 | |||||||
chr11:17780947 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1694-723G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780947 | |||||||
chr11:17780957 | G | T | 1 | a0001c0001t0002g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1694-713G>T | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780957 | |||||||
chr11:17780978 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1694-692G>A | KCNC1 | ENSG00000129159.9 | transcript | ENST00000265969.8 | protein_coding | 3/3 | chr11 | 17780978 |