geneid | 285172 |
---|---|
ensemblid | ENSG00000155744.10 |
hgncid | 28593 |
symbol | HYCC2 |
name | hyccin PI4KA lipid kinase complex subunit 2 |
refseq_nuc | NM_001321623.1 |
refseq_prot | NP_001308552.1 |
ensembl_nuc | ENST00000681958.1 |
ensembl_prot | ENSP00000507218.1 |
mane_status | MANE Select |
chr | chr2 |
start | 200973718 |
end | 201071671 |
strand | - |
ver | v1.2 |
region | chr2:200973718-201071671 |
region5000 | chr2:200968718-201076671 |
regionname0 | HYCC2_chr2_200973718_201071671 |
regionname5000 | HYCC2_chr2_200968718_201076671 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 586 | 175 | 85 | 38 | 24 | 10 | 16 | 8 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0002 | 0/0 | 586 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 7743 | 44 | 9 | 17 | 11 | 2 | 3 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0002 | 0/0 | 7741 | 16 | 3 | 2 | 5 | 1 | 5 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0003 | 0/0 | 7738 | 14 | 14 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0004 | 0/0 | 7738 | 12 | 8 | 2 | 1 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0005 | 0/0 | 7733 | 9 | 9 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0006 | 0/0 | 7738 | 8 | 0 | 5 | 1 | 2 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0007 | 0/0 | 7744 | 8 | 3 | 3 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0008 | 0/0 | 7740 | 8 | 5 | 3 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0009 | 0/0 | 7745 | 6 | 6 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0010 | 0/0 | 7739 | 4 | 2 | 1 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0011 | 0/0 | 7737 | 4 | 4 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0012 | 0/0 | 7742 | 3 | 2 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0013 | 0/0 | 7740 | 3 | 0 | 1 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0014 | 0/0 | 7736 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0015 | 0/0 | 7743 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0016 | 0/0 | 7743 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0017 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0018 | 0/0 | 7745 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0019 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0020 | 0/0 | 7741 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0021 | 0/0 | 7731 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0022 | 0/0 | 7737 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0023 | 0/0 | 7739 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0024 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0025 | 0/0 | 7736 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0026 | 0/0 | 7741 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0027 | 0/0 | 7739 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0028 | 0/0 | 7739 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0029 | 0/0 | 7738 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0030 | 0/0 | 7743 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0031 | 0/0 | 7741 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0032 | 0/0 | 7741 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0033 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0034 | 0/0 | 7746 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0035 | 0/0 | 7745 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0036 | 0/0 | 7746 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0037 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0038 | 0/0 | 7745 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0039 | 0/0 | 7745 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0040 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0041 | 0/0 | 7737 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0042 | 0/0 | 7743 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0043 | 0/0 | 7736 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0044 | 0/0 | 7743 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
t0045 | 0/0 | 7738 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1761 | 175 | 85 | 38 | 24 | 10 | 16 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0002c0002 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 9503 | 44 | 9 | 17 | 11 | 2 | 3 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0002 | 0/0 | 9501 | 16 | 3 | 2 | 5 | 1 | 5 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0003 | 0/0 | 9498 | 14 | 14 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0004 | 0/0 | 9498 | 12 | 8 | 2 | 1 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0005 | 0/0 | 9493 | 8 | 8 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0006 | 0/0 | 9498 | 8 | 0 | 5 | 1 | 2 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0007 | 0/0 | 9504 | 8 | 3 | 3 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0008 | 0/0 | 9500 | 8 | 5 | 3 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0009 | 0/0 | 9505 | 6 | 6 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0010 | 0/0 | 9499 | 4 | 2 | 1 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0011 | 0/0 | 9497 | 4 | 4 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0012 | 0/0 | 9502 | 3 | 2 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0013 | 0/0 | 9500 | 3 | 0 | 1 | 0 | 1 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0014 | 0/0 | 9496 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0015 | 0/0 | 9503 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0016 | 0/0 | 9503 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0017 | 0/0 | 9500 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0018 | 0/0 | 9505 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0019 | 0/0 | 9497 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0020 | 0/0 | 9501 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0021 | 0/0 | 9491 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0022 | 0/0 | 9497 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0023 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0024 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0025 | 0/0 | 9496 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0026 | 0/0 | 9501 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0027 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0028 | 0/0 | 9499 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0029 | 0/0 | 9498 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0030 | 0/0 | 9503 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0031 | 0/0 | 9501 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0032 | 0/0 | 9501 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0033 | 0/0 | 9500 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0034 | 0/0 | 9506 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0035 | 0/0 | 9505 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0036 | 0/0 | 9506 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0037 | 0/0 | 9505 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0038 | 0/0 | 9505 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0039 | 0/0 | 9505 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0040 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0041 | 0/0 | 9497 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0042 | 0/0 | 9503 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0043 | 0/0 | 9496 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0044 | 0/0 | 9503 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0001c0001t0045 | 0/0 | 9498 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
a0002c0002t0005 | 0/0 | 9493 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | copy fasta | chr2 | 200968718 | 201076671 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0017 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0011g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0011g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0013g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0013g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0014g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0015g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0015g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0016g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0018g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0020g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0021g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0022g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0023g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0024g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0027g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0028g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0029g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0030g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0031g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0034g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0035g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0036g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0037g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0038g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0039g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0040g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0041g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0042g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0043g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0044g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0001c0001t0045g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
a0002c0002t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0037 | g0083 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0077 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00140 | hp2 | a0001 | c0001 | t0042 | g0060 | EUR | GBR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0119 | EUR | FIN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00408 | hp1 | a0001 | c0001 | t0018 | g0062 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00408 | hp2 | a0001 | c0001 | t0020 | g0059 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00642 | hp2 | a0001 | c0001 | t0015 | g0056 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00741 | hp1 | a0001 | c0001 | t0036 | g0080 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01069 | hp2 | a0001 | c0001 | t0035 | g0143 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0142 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01071 | hp2 | a0001 | c0001 | t0010 | g0063 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0171 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0138 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0100 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01261 | hp1 | a0001 | c0001 | t0013 | g0145 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0107 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0118 | EUR | IBS | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01952 | hp2 | a0001 | c0001 | t0015 | g0006 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0106 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0025 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02055 | hp1 | a0001 | c0001 | t0023 | g0137 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0087 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02080 | hp1 | a0001 | c0001 | t0029 | g0123 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02132 | hp1 | a0001 | c0001 | t0030 | g0037 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02145 | hp1 | a0001 | c0001 | t0044 | g0096 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02145 | hp2 | a0001 | c0001 | t0028 | g0144 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0122 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0092 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02280 | hp1 | a0001 | c0001 | t0021 | g0174 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0116 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0139 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02622 | hp1 | a0001 | c0001 | t0040 | g0164 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02630 | hp1 | a0001 | c0001 | t0041 | g0160 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0140 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0050 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02717 | hp2 | a0001 | c0001 | t0043 | g0146 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02723 | hp1 | a0001 | c0001 | t0019 | g0018 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0064 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02735 | hp2 | a0001 | c0001 | t0033 | g0126 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0168 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0149 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0167 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0125 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03130 | hp2 | a0001 | c0001 | t0038 | g0047 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0151 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0114 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0115 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03225 | hp1 | a0001 | c0001 | t0034 | g0172 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03453 | hp2 | a0001 | c0001 | t0024 | g0166 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0155 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03491 | hp2 | a0001 | c0001 | t0013 | g0005 | SAS | PJL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0111 | AFR | ESN | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0159 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03927 | hp1 | a0001 | c0001 | t0039 | g0079 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03942 | hp1 | a0001 | c0001 | t0022 | g0094 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03942 | hp2 | a0001 | c0001 | t0032 | g0004 | SAS | BEB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG04115 | hp2 | a0001 | c0001 | t0012 | g0039 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | YRI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18944 | hp2 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA18979 | hp2 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19043 | hp2 | a0001 | c0001 | t0031 | g0091 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA20752 | hp1 | a0001 | c0001 | t0013 | g0003 | EUR | TSI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA20752 | hp2 | a0001 | c0001 | t0010 | g0054 | EUR | TSI | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02109 | hp1 | a0001 | c0001 | t0027 | g0033 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02486 | hp1 | a0001 | c0001 | t0026 | g0113 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02486 | hp2 | a0001 | c0001 | t0045 | g0130 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0002 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0170 | AFR | ACB | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
HG06807 | hp2 | a0001 | c0001 | t0017 | g0150 | AFR | USA | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0075 | REF | REF | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | HYCC2_chr2_200968718_201076671 | HYCC2 | chr2 | 200968718 | 201076671 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200992939
|
C | A | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.691G>T | p.Val231Leu | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/13 | 881/9503 | 691/1761 | 231/586 | chr2 | 200992939 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200974210
|
TA | T | 3 | a0001c0001t0011a0001c0001t0040a0001c0001t0041 | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7059delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 7059 | chr2 | 200974210 | |||||
chr2:200974268
|
G | A | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7002C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 7002 | chr2 | 200974268 | |||||
chr2:200974355
|
G | C | 1 | a0001c0001t0024 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6915C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6915 | chr2 | 200974355 | |||||
chr2:200974482
|
A | G | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6788T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6788 | chr2 | 200974482 | |||||
chr2:200974529
|
A | G | 1 | a0001c0001t0016 | 2 | NA18944.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6741T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6741 | chr2 | 200974529 | |||||
chr2:200974797
|
T | C | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6473A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6473 | chr2 | 200974797 | |||||
chr2:200974872
|
A | G | 2 | a0001c0001t0021a0001c0001t0034 | 2 | HG02280.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6398T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6398 | chr2 | 200974872 | |||||
chr2:200974931
|
T | C | 2 | a0001c0001t0014a0001c0001t0043 | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6339A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6339 | chr2 | 200974931 | |||||
chr2:200975057
|
T | A | 1 | a0001c0001t0029 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6213A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6213 | chr2 | 200975057 | |||||
chr2:200975232
|
T | C | 1 | a0001c0001t0037 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6038A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6038 | chr2 | 200975232 | |||||
chr2:200975252
|
C | T | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6018G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 6018 | chr2 | 200975252 | |||||
chr2:200975360
|
C | T | 1 | a0001c0001t0033 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5910G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5910 | chr2 | 200975360 | |||||
chr2:200975370
|
T | C | 2 | a0001c0001t0005a0002c0002t0005 | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5900A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5900 | chr2 | 200975370 | |||||
chr2:200975541
|
T | A | 1 | a0001c0001t0038 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5729A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5729 | chr2 | 200975541 | |||||
chr2:200975669
|
A | G | 1 | a0001c0001t0026 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5601T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5601 | chr2 | 200975669 | |||||
chr2:200975968
|
T | A | 1 | a0001c0001t0026 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5302A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5302 | chr2 | 200975968 | |||||
chr2:200976197
|
A | C | 2 | a0001c0001t0005a0002c0002t0005 | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5073T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5073 | chr2 | 200976197 | |||||
chr2:200976207
|
T | G | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5063A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 5063 | chr2 | 200976207 | |||||
chr2:200976757
|
A | G | 2 | a0001c0001t0027a0001c0001t0031 | 2 | HG02109.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4513T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4513 | chr2 | 200976757 | |||||
chr2:200976782
|
T | C | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4488A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4488 | chr2 | 200976782 | |||||
chr2:200977128
|
T | C | 1 | a0001c0001t0039 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4142A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 4142 | chr2 | 200977128 | |||||
chr2:200977285
|
G | C | 1 | a0001c0001t0030 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3985C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3985 | chr2 | 200977285 | |||||
chr2:200977287
|
G | A | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(5): Show | 33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3983C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3983 | chr2 | 200977287 | |||||
chr2:200977778
|
G | A | 3 | a0001c0001t0011a0001c0001t0040a0001c0001t0041 | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3492C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3492 | chr2 | 200977778 | |||||
chr2:200977991
|
C | T | 1 | a0001c0001t0017 | 2 | HG02965.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3279G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3279 | chr2 | 200977991 | |||||
chr2:200978126
|
T | A | 1 | a0001c0001t0006 | 8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3144A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3144 | chr2 | 200978126 | |||||
chr2:200978127
|
A | C | 1 | a0001c0001t0006 | 8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3143T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 3143 | chr2 | 200978127 | |||||
chr2:200978464
|
C | CT | 4 | a0001c0001t0007a0001c0001t0012a0001c0001t0034others(1): Show | 13 | HG00140.hp1 HG00741.hp1 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2805dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2805 | chr2 | 200978464 | |||||
chr2:200978464
|
CTT | C | 10 | a0001c0001t0014a0001c0001t0019a0001c0001t0021others(7): Show | 12 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805delAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2804 | chr2 | 200978464 | |||||
chr2:200978464
|
CTTT | C | 5 | a0001c0001t0003a0001c0001t0011a0001c0001t0013others(2): Show | 23 | HG01261.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2803_*2805delAAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2803 | chr2 | 200978464 | |||||
chr2:200978464
|
CTTTT | C | 2 | a0001c0001t0005a0002c0002t0005 | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2802_*2805delAAAA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2802 | chr2 | 200978464 | |||||
chr2:200978464
|
CTTTTT | C | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(5): Show | 34 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2801_*2805delAAAA others(1): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2801 | chr2 | 200978464 | |||||
chr2:200978534
|
A | G | 21 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(18): Show | 72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2736T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2736 | chr2 | 200978534 | |||||
chr2:200978761
|
C | T | 1 | a0001c0001t0033 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2509G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2509 | chr2 | 200978761 | |||||
chr2:200978807
|
G | A | 4 | a0001c0001t0013a0001c0001t0019a0001c0001t0028others(1): Show | 6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2463C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2463 | chr2 | 200978807 | |||||
chr2:200979247
|
T | C | 1 | a0001c0001t0022 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2023A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2023 | chr2 | 200979247 | |||||
chr2:200979264
|
T | TAC | 11 | a0001c0001t0008a0001c0001t0009a0001c0001t0017others(8): Show | 24 | HG00099.hp1 HG00408.hp1 HG00741.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2005dupGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2005 | chr2 | 200979264 | |||||
chr2:200979264
|
TAC | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(10): Show | 46 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2004_*2005delGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2004 | chr2 | 200979264 | |||||
chr2:200979264
|
TACAC | T | 4 | a0001c0001t0010a0001c0001t0014a0001c0001t0019others(1): Show | 9 | HG01071.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2005delGTGT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2002 | chr2 | 200979264 | |||||
chr2:200979264
|
TACACAC | T | 3 | a0001c0001t0005a0001c0001t0022a0002c0002t0005 | 10 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2000_*2005delGTGT others(2): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 2000 | chr2 | 200979264 | |||||
chr2:200979264
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996_*2005delGTGT others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1996 | chr2 | 200979264 | |||||
chr2:200979286
|
C | T | 1 | a0001c0001t0020 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1984G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1984 | chr2 | 200979286 | |||||
chr2:200979525
|
T | C | 1 | a0001c0001t0014 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1745A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1745 | chr2 | 200979525 | |||||
chr2:200979828
|
C | A | 3 | a0001c0001t0011a0001c0001t0040a0001c0001t0041 | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1442G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1442 | chr2 | 200979828 | |||||
chr2:200979929
|
G | A | 1 | a0001c0001t0042 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1341C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1341 | chr2 | 200979929 | |||||
chr2:200979948
|
A | G | 1 | a0001c0001t0043 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1322 | chr2 | 200979948 | |||||
chr2:200980061
|
CT | C | 2 | a0001c0001t0014a0001c0001t0043 | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 1208 | chr2 | 200980061 | |||||
chr2:200980485
|
T | A | 1 | a0001c0001t0044 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 785 | chr2 | 200980485 | |||||
chr2:200980533
|
C | T | 1 | a0001c0001t0019 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 737 | chr2 | 200980533 | |||||
chr2:200980680
|
G | T | 1 | a0001c0001t0015 | 2 | HG00642.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*590C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 590 | chr2 | 200980680 | |||||
chr2:200980933
|
C | G | 1 | a0001c0001t0018 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 337 | chr2 | 200980933 | |||||
chr2:200980986
|
T | C | 1 | a0001c0001t0045 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*284A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 13/13 | 284 | chr2 | 200980986 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:200982084
|
T | C | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1160-213A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982084 | ||||||
chr2:200982196
|
ATTC | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1160-328_1160-326d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982196 | ||||||
chr2:200982204
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-333A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982204 | ||||||
chr2:200982214
|
C | T | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-343G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982214 | ||||||
chr2:200982230
|
GAAAAA | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-364_1160-360d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982230 | ||||||
chr2:200982308
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1160-437A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982308 | ||||||
chr2:200982536
|
T | C | 4 | a0001c0001t0004g0001a0001c0001t0004g0090a0001c0001t0004g0109others(1): Show | 5 | HG01891.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1160-665A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982536 | ||||||
chr2:200982703
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1160-832G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982703 | ||||||
chr2:200982883
|
G | A | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1160-1012C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982883 | ||||||
chr2:200982979
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0018g0062 | 2 | HG00408.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1160-1108C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200982979 | ||||||
chr2:200983047
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1160-1176G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983047 | ||||||
chr2:200983154
|
A | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1160-1283T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983154 | ||||||
chr2:200983163
|
G | C | 124 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1160-1292C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983163 | ||||||
chr2:200983167
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-1296T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983167 | ||||||
chr2:200983666
|
CAT | C | 54 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(51): Show | 56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1160-1797_1160-179 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983666 | ||||||
chr2:200983797
|
G | T | 6 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0154others(3): Show | 6 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-1926C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200983797 | ||||||
chr2:200984390
|
C | G | 23 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(20): Show | 23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.1160-2519G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984390 | ||||||
chr2:200984545
|
G | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1160-2674C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984545 | ||||||
chr2:200984987
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1159+2378A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200984987 | ||||||
chr2:200985532
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1159+1833C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985532 | ||||||
chr2:200985591
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1159+1774C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985591 | ||||||
chr2:200985792
|
A | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1159+1573T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985792 | ||||||
chr2:200985833
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1159+1532G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985833 | ||||||
chr2:200985834
|
T | A | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1159+1531A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985834 | ||||||
chr2:200985873
|
T | C | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1159+1492A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985873 | ||||||
chr2:200985932
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+1433T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200985932 | ||||||
chr2:200986382
|
T | C | 10 | a0001c0001t0003g0036a0001c0001t0003g0120a0001c0001t0003g0127others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1159+983A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986382 | ||||||
chr2:200986508
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1159+857A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986508 | ||||||
chr2:200986834
|
T | C | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+531A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200986834 | ||||||
chr2:200987043
|
A | G | 3 | a0001c0001t0004g0121a0001c0001t0004g0124a0001c0001t0025g0114 | 3 | HG02922.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1159+322T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 12/12 | chr2 | 200987043 | ||||||
chr2:200988734
|
A | G | 54 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(51): Show | 56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.832-313T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200988734 | ||||||
chr2:200989107
|
A | G | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(3): Show | 6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-686T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989107 | ||||||
chr2:200989222
|
A | G | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-801T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989222 | ||||||
chr2:200989350
|
T | C | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.832-929A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989350 | ||||||
chr2:200989452
|
C | A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.832-1031G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989452 | ||||||
chr2:200989471
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-1050A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989471 | ||||||
chr2:200989651
|
A | G | 1 | a0001c0001t0010g0063 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.832-1230T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989651 | ||||||
chr2:200989913
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.832-1492T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200989913 | ||||||
chr2:200990277
|
T | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-1856A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990277 | ||||||
chr2:200990475
|
T | C | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+1806A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990475 | ||||||
chr2:200990579
|
CT | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+1701delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990579 | ||||||
chr2:200990590
|
T | C | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+1691A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990590 | ||||||
chr2:200990621
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+1660C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990621 | ||||||
chr2:200990665
|
C | T | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+1616G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990665 | ||||||
chr2:200990680
|
C | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+1601G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990680 | ||||||
chr2:200990831
|
G | A | 79 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(76): Show | 81 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+1450C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200990831 | ||||||
chr2:200991315
|
C | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.831+966G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991315 | ||||||
chr2:200991420
|
T | C | 1 | a0001c0001t0038g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+861A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991420 | ||||||
chr2:200991568
|
C | CA | 13 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0043others(10): Show | 13 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+712dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991568 | ||||||
chr2:200991645
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+636C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991645 | ||||||
chr2:200991645
|
G | T | 1 | a0001c0001t0038g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+636C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991645 | ||||||
chr2:200991754
|
A | AAAAT | 71 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(68): Show | 73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.831+523_831+526dup others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991754 | ||||||
chr2:200991784
|
G | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+497C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991784 | ||||||
chr2:200991896
|
C | A | 1 | a0001c0001t0012g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.831+385G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991896 | ||||||
chr2:200991937
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.831+344C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200991937 | ||||||
chr2:200992008
|
T | G | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+273A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200992008 | ||||||
chr2:200992143
|
G | T | 1 | a0001c0001t0002g0015 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.831+138C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 10/12 | chr2 | 200992143 | ||||||
chr2:200992379
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.744-11C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992379 | ||||||
chr2:200992413
|
C | T | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(3): Show | 6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-45G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992413 | ||||||
chr2:200992599
|
A | T | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.744-231T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992599 | ||||||
chr2:200992809
|
G | A | 1 | a0002c0002t0005g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.743+78C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 9/12 | chr2 | 200992809 | ||||||
chr2:200993106
|
A | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.627-103T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993106 | ||||||
chr2:200993194
|
A | G | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-191T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993194 | ||||||
chr2:200993818
|
A | G | 1 | a0001c0001t0042g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.627-815T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993818 | ||||||
chr2:200993925
|
A | G | 71 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(68): Show | 73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.627-922T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993925 | ||||||
chr2:200993999
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.627-996C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200993999 | ||||||
chr2:200994192
|
G | C | 1 | a0001c0001t0001g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-1189C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994192 | ||||||
chr2:200994277
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.627-1274G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994277 | ||||||
chr2:200994527
|
G | A | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.627-1524C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994527 | ||||||
chr2:200994687
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.627-1684C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994687 | ||||||
chr2:200994836
|
A | G | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.627-1833T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200994836 | ||||||
chr2:200995290
|
T | C | 1 | a0001c0001t0029g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.626+2155A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995290 | ||||||
chr2:200995366
|
A | G | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.626+2079T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995366 | ||||||
chr2:200995401
|
TC | T | 4 | a0001c0001t0006g0104a0001c0001t0006g0107a0001c0001t0006g0108others(1): Show | 4 | HG00741.hp2 HG01168.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+2043delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995401 | ||||||
chr2:200995426
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+2019G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200995426 | ||||||
chr2:200996028
|
C | CT | 24 | a0001c0001t0001g0061a0001c0001t0001g0102a0001c0001t0002g0015others(21): Show | 24 | HG00408.hp2 HG00738.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+1416dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996028 | ||||||
chr2:200996028
|
CT | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0136a0001c0001t0005g0019others(8): Show | 11 | HG02280.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+1416delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996028 | ||||||
chr2:200996093
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.626+1352C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996093 | ||||||
chr2:200996465
|
T | TA | 11 | a0001c0001t0001g0093a0001c0001t0005g0019a0001c0001t0005g0147others(8): Show | 11 | HG01192.hp2 HG01261.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+979dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996465 | ||||||
chr2:200996581
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.626+864G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996581 | ||||||
chr2:200996769
|
T | C | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.626+676A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996769 | ||||||
chr2:200996824
|
C | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.626+621G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996824 | ||||||
chr2:200996899
|
C | G | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.626+546G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996899 | ||||||
chr2:200996971
|
A | G | 23 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(20): Show | 23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.626+474T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200996971 | ||||||
chr2:200997272
|
C | T | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.626+173G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200997272 | ||||||
chr2:200997429
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0007g0100 | 3 | HG01069.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.626+16A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 8/12 | chr2 | 200997429 | ||||||
chr2:200997705
|
A | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-165T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200997705 | ||||||
chr2:200997813
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-273C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200997813 | ||||||
chr2:200998245
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.531-705A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998245 | ||||||
chr2:200998412
|
T | C | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.531-872A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998412 | ||||||
chr2:200998491
|
C | T | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.531-951G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998491 | ||||||
chr2:200998577
|
C | T | 5 | a0001c0001t0001g0075a0001c0001t0001g0098a0001c0001t0001g0101others(2): Show | 5 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-1037G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998577 | ||||||
chr2:200998618
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.531-1078C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998618 | ||||||
chr2:200998807
|
T | C | 83 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(80): Show | 85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.531-1267A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200998807 | ||||||
chr2:200999080
|
C | A | 71 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(68): Show | 73 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.531-1540G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999080 | ||||||
chr2:200999454
|
C | G | 1 | a0001c0001t0007g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.531-1914G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999454 | ||||||
chr2:200999472
|
G | A | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.531-1932C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999472 | ||||||
chr2:200999575
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.531-2035G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999575 | ||||||
chr2:200999818
|
C | T | 6 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0154others(3): Show | 6 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.531-2278G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999818 | ||||||
chr2:200999834
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.531-2294G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999834 | ||||||
chr2:200999927
|
G | A | 20 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0075others(17): Show | 20 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(17): Show |
intron_variant | MODIFIER | c.531-2387C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999927 | ||||||
chr2:200999977
|
G | A | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.531-2437C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 200999977 | ||||||
chr2:201000057
|
C | CA | 12 | a0001c0001t0001g0022a0001c0001t0001g0066a0001c0001t0003g0127others(9): Show | 12 | HG00733.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.531-2518dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | ||||||
chr2:201000057
|
C | CAAA | 7 | a0001c0001t0005g0019a0001c0001t0005g0148a0001c0001t0005g0152others(4): Show | 7 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.531-2520_531-2518d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | ||||||
chr2:201000057
|
CA | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0038a0001c0001t0001g0061others(7): Show | 10 | HG00408.hp1 HG01257.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-2518delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000057 | ||||||
chr2:201000124
|
C | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-2584G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000124 | ||||||
chr2:201000127
|
T | C | 1 | a0001c0001t0009g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.531-2587A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000127 | ||||||
chr2:201000319
|
G | T | 2 | a0001c0001t0013g0005a0001c0001t0032g0004 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.531-2779C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000319 | ||||||
chr2:201000436
|
G | T | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-2896C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000436 | ||||||
chr2:201000469
|
G | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.531-2929C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000469 | ||||||
chr2:201000588
|
AG | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.531-3049delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000588 | ||||||
chr2:201000706
|
T | C | 6 | a0001c0001t0008g0002a0001c0001t0008g0111a0001c0001t0008g0115others(3): Show | 7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-3166A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000706 | ||||||
chr2:201000836
|
AG | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-3297delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000836 | ||||||
chr2:201000960
|
C | T | 1 | a0001c0001t0043g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531-3420G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000960 | ||||||
chr2:201000970
|
C | CA | 10 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0003g0165others(7): Show | 10 | HG00642.hp2 HG00738.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-3431dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201000970 | ||||||
chr2:201001022
|
C | T | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.531-3482G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001022 | ||||||
chr2:201001121
|
G | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531-3581C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001121 | ||||||
chr2:201001135
|
C | G | 1 | a0001c0001t0044g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531-3595G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001135 | ||||||
chr2:201001137
|
C | CA | 22 | a0001c0001t0001g0028a0001c0001t0004g0117a0001c0001t0005g0019others(19): Show | 22 | HG01261.hp1 HG01515.hp2 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-3598dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001137 | ||||||
chr2:201001147
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531-3607T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001147 | ||||||
chr2:201001260
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-3720T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001260 | ||||||
chr2:201001530
|
C | T | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-3990G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001530 | ||||||
chr2:201001642
|
T | C | 1 | a0001c0001t0007g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.531-4102A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001642 | ||||||
chr2:201001685
|
T | G | 23 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(20): Show | 23 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(20): Show |
intron_variant | MODIFIER | c.531-4145A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001685 | ||||||
chr2:201001702
|
C | A | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.531-4162G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001702 | ||||||
chr2:201001987
|
T | G | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.531-4447A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201001987 | ||||||
chr2:201002149
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.531-4609A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002149 | ||||||
chr2:201002273
|
C | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.531-4733G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002273 | ||||||
chr2:201002281
|
C | CA | 26 | a0001c0001t0001g0038a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 26 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.531-4742dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002281 | ||||||
chr2:201002629
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.531-5089C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002629 | ||||||
chr2:201002775
|
G | A | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.531-5235C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002775 | ||||||
chr2:201002870
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.531-5330T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002870 | ||||||
chr2:201002891
|
G | A | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.531-5351C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002891 | ||||||
chr2:201002906
|
A | G | 1 | a0001c0001t0007g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.531-5366T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201002906 | ||||||
chr2:201003050
|
G | A | 1 | a0001c0001t0044g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.531-5510C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003050 | ||||||
chr2:201003317
|
A | G | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+5656T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003317 | ||||||
chr2:201003372
|
G | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530+5601C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003372 | ||||||
chr2:201003439
|
G | A | 3 | a0001c0001t0017g0149a0001c0001t0017g0150a0001c0001t0034g0172 | 3 | HG02965.hp1 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+5534C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003439 | ||||||
chr2:201003578
|
G | A | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+5395C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003578 | ||||||
chr2:201003582
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0007g0025 | 2 | HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.530+5391C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003582 | ||||||
chr2:201003805
|
C | CT | 18 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0038others(15): Show | 18 | HG00642.hp2 HG00741.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.530+5167dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | ||||||
chr2:201003805
|
CT | C | 57 | a0001c0001t0001g0157a0001c0001t0002g0158a0001c0001t0003g0036others(54): Show | 59 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.530+5167delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | ||||||
chr2:201003805
|
CTT | C | 9 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(6): Show | 9 | HG01261.hp1 HG02080.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.530+5166_530+5167d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | ||||||
chr2:201003805
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0065 | 3 | HG01496.hp1 HG01515.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.530+5156_530+5167d others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003805 | ||||||
chr2:201003970
|
C | G | 4 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(1): Show | 4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+5003G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201003970 | ||||||
chr2:201004005
|
G | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+4968C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004005 | ||||||
chr2:201004021
|
G | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.530+4952C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004021 | ||||||
chr2:201004134
|
C | T | 6 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0035others(3): Show | 6 | HG03017.hp2 HG03834.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+4839G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004134 | ||||||
chr2:201004307
|
G | A | 6 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(3): Show | 6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+4666C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004307 | ||||||
chr2:201004396
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+4577A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004396 | ||||||
chr2:201004447
|
C | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02615.hp1 HG02615.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+4526G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004447 | ||||||
chr2:201004679
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.530+4294G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004679 | ||||||
chr2:201004768
|
G | A | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.530+4205C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004768 | ||||||
chr2:201004799
|
C | T | 15 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(12): Show | 15 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+4174G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201004799 | ||||||
chr2:201005016
|
C | CA | 34 | a0001c0001t0002g0015a0001c0001t0004g0001a0001c0001t0004g0089others(31): Show | 36 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.530+3956dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005016 | ||||||
chr2:201005096
|
G | A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+3877C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005096 | ||||||
chr2:201005232
|
G | A | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.530+3741C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005232 | ||||||
chr2:201005559
|
A | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+3414T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005559 | ||||||
chr2:201005721
|
C | T | 1 | a0001c0001t0011g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+3252G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005721 | ||||||
chr2:201005765
|
G | A | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.530+3208C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201005765 | ||||||
chr2:201006026
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+2947C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006026 | ||||||
chr2:201006130
|
C | CT | 16 | a0001c0001t0003g0120a0001c0001t0003g0135a0001c0001t0004g0132others(13): Show | 16 | HG01975.hp2 HG02027.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.530+2842dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006130 | ||||||
chr2:201006188
|
C | T | 1 | a0001c0001t0014g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.530+2785G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006188 | ||||||
chr2:201006295
|
A | AT | 19 | a0001c0001t0001g0043a0001c0001t0001g0076a0001c0001t0002g0035others(16): Show | 19 | HG02080.hp1 HG02145.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+2677dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006295 | ||||||
chr2:201006295
|
AT | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(3): Show | 6 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.530+2677delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006295 | ||||||
chr2:201006426
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.530+2547G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006426 | ||||||
chr2:201006682
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.530+2291A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006682 | ||||||
chr2:201006781
|
G | A | 2 | a0001c0001t0009g0032a0001c0001t0009g0048 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.530+2192C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006781 | ||||||
chr2:201006947
|
A | T | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+2026T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201006947 | ||||||
chr2:201007129
|
C | T | 1 | a0001c0001t0004g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.530+1844G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007129 | ||||||
chr2:201007222
|
A | G | 1 | a0001c0001t0006g0112 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.530+1751T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007222 | ||||||
chr2:201007233
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+1740G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007233 | ||||||
chr2:201007245
|
C | T | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.530+1728G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007245 | ||||||
chr2:201007250
|
A | G | 1 | a0001c0001t0004g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.530+1723T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007250 | ||||||
chr2:201007255
|
A | G | 54 | a0001c0001t0002g0158a0001c0001t0003g0036a0001c0001t0003g0120others(51): Show | 56 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.530+1718T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007255 | ||||||
chr2:201007288
|
A | G | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1685T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007288 | ||||||
chr2:201007327
|
C | T | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1646G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007327 | ||||||
chr2:201007457
|
T | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1516A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007457 | ||||||
chr2:201007537
|
G | A | 1 | a0001c0001t0011g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+1436C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007537 | ||||||
chr2:201007641
|
C | T | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1332G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007641 | ||||||
chr2:201007731
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+1242C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007731 | ||||||
chr2:201007772
|
A | G | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+1201T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007772 | ||||||
chr2:201007784
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.530+1189T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007784 | ||||||
chr2:201007969
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.530+1004A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201007969 | ||||||
chr2:201008184
|
C | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+789G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008184 | ||||||
chr2:201008530
|
T | G | 1 | a0001c0001t0004g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.530+443A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008530 | ||||||
chr2:201008595
|
T | TAAATAAA others(13): Show |
9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+358_530+377dup others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008595 | ||||||
chr2:201008687
|
G | A | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.530+286C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008687 | ||||||
chr2:201008918
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.530+55A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 7/12 | chr2 | 201008918 | ||||||
chr2:201009331
|
A | G | 1 | a0001c0001t0043g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415-243T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009331 | ||||||
chr2:201009648
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.415-560G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009648 | ||||||
chr2:201009742
|
G | A | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415-654C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009742 | ||||||
chr2:201009852
|
C | G | 1 | a0001c0001t0008g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.415-764G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009852 | ||||||
chr2:201009864
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.415-776C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009864 | ||||||
chr2:201009997
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.415-909C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201009997 | ||||||
chr2:201010014
|
G | A | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-926C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010014 | ||||||
chr2:201010103
|
C | CA | 6 | a0001c0001t0001g0097a0001c0001t0004g0001a0001c0001t0004g0090others(3): Show | 7 | HG00140.hp1 HG00738.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-1016dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010103 | ||||||
chr2:201010104
|
A | C | 1 | a0001c0001t0036g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.415-1016T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010104 | ||||||
chr2:201010196
|
T | A | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.415-1108A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010196 | ||||||
chr2:201010250
|
G | C | 4 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(1): Show | 4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+1142C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010250 | ||||||
chr2:201010307
|
T | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+1085A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010307 | ||||||
chr2:201010767
|
A | AG | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+624dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010767 | ||||||
chr2:201010786
|
T | C | 6 | a0001c0001t0008g0002a0001c0001t0008g0111a0001c0001t0008g0115others(3): Show | 7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+606A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010786 | ||||||
chr2:201010822
|
T | A | 1 | a0001c0001t0007g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.414+570A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010822 | ||||||
chr2:201010917
|
C | T | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+475G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010917 | ||||||
chr2:201010931
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414+461C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201010931 | ||||||
chr2:201011087
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414+305C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201011087 | ||||||
chr2:201011329
|
C | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+63G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 6/12 | chr2 | 201011329 | ||||||
chr2:201011804
|
A | C | 1 | a0001c0001t0013g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-332T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011804 | ||||||
chr2:201011833
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-361G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011833 | ||||||
chr2:201011954
|
A | T | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.334-482T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201011954 | ||||||
chr2:201012259
|
A | T | 1 | a0001c0001t0005g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-787T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012259 | ||||||
chr2:201012347
|
G | A | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-875C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012347 | ||||||
chr2:201012398
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-926A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012398 | ||||||
chr2:201012593
|
A | G | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-1121T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012593 | ||||||
chr2:201012834
|
A | G | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.334-1362T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012834 | ||||||
chr2:201012952
|
T | TAC | 6 | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0007g0045others(3): Show | 6 | HG00408.hp1 HG02132.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1482_334-1481d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | ||||||
chr2:201012952
|
TAC | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 88 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.334-1482_334-1481d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | ||||||
chr2:201012952
|
TACAC | T | 17 | a0001c0001t0001g0038a0001c0001t0001g0157a0001c0001t0002g0020others(14): Show | 17 | HG01261.hp1 HG01496.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.334-1484_334-1481d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | ||||||
chr2:201012952
|
TACACAC | T | 10 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(7): Show | 10 | HG02615.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.334-1486_334-1481d others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | ||||||
chr2:201012952
|
TACACACA others(1): Show |
T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-1488_334-1481d others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201012952 | ||||||
chr2:201013158
|
G | A | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-1686C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013158 | ||||||
chr2:201013163
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-1691T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013163 | ||||||
chr2:201013436
|
T | G | 1 | a0001c0001t0002g0021 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-1964A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013436 | ||||||
chr2:201013479
|
CA | C | 5 | a0001c0001t0006g0118a0001c0001t0007g0077a0001c0001t0011g0167others(2): Show | 5 | HG00140.hp1 HG01069.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2008delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013479 | ||||||
chr2:201013483
|
A | C | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.334-2011T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013483 | ||||||
chr2:201013523
|
T | A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2051A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013523 | ||||||
chr2:201013526
|
C | CCAAACAC others(1): Show |
2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.334-2062_334-2055d others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013526 | ||||||
chr2:201013547
|
C | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-2075G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013547 | ||||||
chr2:201013580
|
G | A | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.334-2108C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013580 | ||||||
chr2:201013593
|
A | G | 1 | a0001c0001t0005g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.334-2121T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013593 | ||||||
chr2:201013664
|
G | A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2192C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013664 | ||||||
chr2:201013670
|
C | G | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.334-2198G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013670 | ||||||
chr2:201013829
|
G | T | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2357C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201013829 | ||||||
chr2:201014078
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-2606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014078 | ||||||
chr2:201014205
|
A | G | 1 | a0001c0001t0004g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.334-2733T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014205 | ||||||
chr2:201014323
|
G | GAT | 173 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.333+2666_333+2667d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014323 | ||||||
chr2:201014366
|
C | T | 1 | a0001c0001t0009g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.333+2625G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014366 | ||||||
chr2:201014669
|
G | A | 1 | a0001c0001t0045g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.333+2322C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014669 | ||||||
chr2:201014732
|
T | C | 14 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(11): Show | 14 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+2259A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201014732 | ||||||
chr2:201015058
|
T | G | 2 | a0001c0001t0001g0023a0001c0001t0015g0056 | 2 | HG00642.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.333+1933A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015058 | ||||||
chr2:201015058
|
TC | T | 6 | a0001c0001t0011g0159a0001c0001t0011g0167a0001c0001t0011g0168others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+1932delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015058 | ||||||
chr2:201015170
|
T | C | 1 | a0001c0001t0014g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.333+1821A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015170 | ||||||
chr2:201015204
|
A | G | 1 | a0001c0001t0001g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.333+1787T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015204 | ||||||
chr2:201015225
|
A | G | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.333+1766T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015225 | ||||||
chr2:201015382
|
T | TTTC | 14 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(11): Show | 14 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+1608_333+1609i others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015382 | ||||||
chr2:201015560
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.333+1431C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015560 | ||||||
chr2:201015661
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.333+1330A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015661 | ||||||
chr2:201015790
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+1201G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015790 | ||||||
chr2:201015833
|
G | A | 1 | a0001c0001t0013g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.333+1158C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015833 | ||||||
chr2:201015834
|
C | T | 1 | a0001c0001t0013g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.333+1157G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201015834 | ||||||
chr2:201016201
|
AAATAC | A | 21 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(18): Show | 21 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+785_333+789del others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016201 | ||||||
chr2:201016230
|
A | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.333+761T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016230 | ||||||
chr2:201016392
|
G | A | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+599C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016392 | ||||||
chr2:201016592
|
A | G | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.333+399T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016592 | ||||||
chr2:201016765
|
A | G | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+226T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016765 | ||||||
chr2:201016770
|
C | T | 83 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(80): Show | 85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.333+221G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016770 | ||||||
chr2:201016804
|
T | A | 1 | a0001c0001t0012g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.333+187A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016804 | ||||||
chr2:201016893
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+98C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016893 | ||||||
chr2:201016954
|
A | G | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.333+37T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 5/12 | chr2 | 201016954 | ||||||
chr2:201017260
|
T | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-90A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017260 | ||||||
chr2:201017314
|
T | G | 1 | a0001c0001t0007g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154-144A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017314 | ||||||
chr2:201017422
|
GATT | G | 3 | a0001c0001t0002g0016a0001c0001t0002g0078a0001c0001t0002g0085 | 3 | HG03017.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.154-255_154-253del others(3): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017422 | ||||||
chr2:201017930
|
C | T | 1 | a0001c0001t0014g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.154-760G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017930 | ||||||
chr2:201017938
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0015g0056 | 2 | HG00642.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.154-768A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017938 | ||||||
chr2:201017961
|
A | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154-791T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201017961 | ||||||
chr2:201018131
|
A | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.154-961T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018131 | ||||||
chr2:201018642
|
T | C | 2 | a0001c0001t0006g0118a0001c0001t0006g0119 | 2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.154-1472A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018642 | ||||||
chr2:201018967
|
C | G | 1 | a0001c0001t0007g0025 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.154-1797G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018967 | ||||||
chr2:201018994
|
T | C | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-1824A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201018994 | ||||||
chr2:201019197
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.154-2027A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019197 | ||||||
chr2:201019215
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.154-2045A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019215 | ||||||
chr2:201019392
|
G | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-2222C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019392 | ||||||
chr2:201019396
|
A | AT | 2 | a0001c0001t0006g0118a0001c0001t0006g0119 | 2 | HG00280.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.154-2227dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019396 | ||||||
chr2:201019418
|
C | T | 1 | a0001c0001t0003g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.154-2248G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019418 | ||||||
chr2:201019438
|
AC | A | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.154-2269delG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019438 | ||||||
chr2:201019502
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.154-2332G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019502 | ||||||
chr2:201019537
|
G | A | 17 | a0001c0001t0001g0173a0001c0001t0002g0015a0001c0001t0002g0016others(14): Show | 17 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-2367C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019537 | ||||||
chr2:201019756
|
T | TA | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-2587dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019756 | ||||||
chr2:201019871
|
C | A | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2701G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019871 | ||||||
chr2:201019954
|
G | A | 1 | a0002c0002t0005g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.154-2784C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201019954 | ||||||
chr2:201020422
|
G | A | 1 | a0001c0001t0003g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153+2409C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020422 | ||||||
chr2:201020543
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153+2288A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020543 | ||||||
chr2:201020570
|
A | T | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.153+2261T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201020570 | ||||||
chr2:201021004
|
T | A | 6 | a0001c0001t0001g0052a0001c0001t0001g0093a0001c0001t0001g0095others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1827A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021004 | ||||||
chr2:201021288
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.153+1543G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021288 | ||||||
chr2:201021635
|
C | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+1196G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021635 | ||||||
chr2:201021833
|
G | A | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.153+998C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021833 | ||||||
chr2:201021945
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.153+886C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201021945 | ||||||
chr2:201022370
|
T | G | 1 | a0001c0001t0004g0125 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.153+461A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022370 | ||||||
chr2:201022443
|
G | A | 1 | a0001c0001t0004g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.153+388C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022443 | ||||||
chr2:201022640
|
T | G | 1 | a0001c0001t0004g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+191A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 4/12 | chr2 | 201022640 | ||||||
chr2:201023504
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.51+455A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023504 | ||||||
chr2:201023594
|
T | C | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.51+365A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023594 | ||||||
chr2:201023607
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.51+352A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023607 | ||||||
chr2:201023713
|
G | A | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.51+246C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023713 | ||||||
chr2:201023807
|
A | T | 1 | a0001c0001t0004g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.51+152T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023807 | ||||||
chr2:201023810
|
C | A | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.51+149G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023810 | ||||||
chr2:201023852
|
TATGTTTC others(15): Show |
T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.51+85_51+106delTAT others(19): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023852 | ||||||
chr2:201023916
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.51+43C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 3/12 | chr2 | 201023916 | ||||||
chr2:201024217
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-178C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024217 | ||||||
chr2:201024375
|
G | A | 31 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0089others(28): Show | 33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30-336C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024375 | ||||||
chr2:201024395
|
C | G | 1 | a0001c0001t0007g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30-356G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024395 | ||||||
chr2:201024418
|
G | A | 1 | a0001c0001t0004g0109 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-30-379C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024418 | ||||||
chr2:201024467
|
C | T | 6 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-428G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024467 | ||||||
chr2:201024940
|
A | G | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-901T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024940 | ||||||
chr2:201024966
|
A | T | 4 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0155others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-927T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201024966 | ||||||
chr2:201025028
|
C | T | 31 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0089others(28): Show | 33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30-989G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025028 | ||||||
chr2:201025169
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-30-1130A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025169 | ||||||
chr2:201025387
|
A | C | 1 | a0001c0001t0014g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-30-1348T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025387 | ||||||
chr2:201025457
|
G | GAAAGA | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-1423_-30-1419d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025457 | ||||||
chr2:201025487
|
A | G | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-1448T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025487 | ||||||
chr2:201025751
|
T | C | 1 | a0001c0001t0045g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-30-1712A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025751 | ||||||
chr2:201025906
|
T | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-1867A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025906 | ||||||
chr2:201025928
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0015g0006 | 3 | HG01192.hp1 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-30-1889C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025928 | ||||||
chr2:201025974
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0012g0087 | 2 | HG00099.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-30-1935A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025974 | ||||||
chr2:201025994
|
G | C | 1 | a0001c0001t0005g0156 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-30-1955C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201025994 | ||||||
chr2:201026081
|
A | T | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-30-2042T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026081 | ||||||
chr2:201026134
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-2095A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026134 | ||||||
chr2:201026169
|
C | A | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-2130G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026169 | ||||||
chr2:201026471
|
A | T | 8 | a0001c0001t0006g0104a0001c0001t0006g0106a0001c0001t0006g0107others(5): Show | 8 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-2432T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026471 | ||||||
chr2:201026574
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-2535G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026574 | ||||||
chr2:201026866
|
A | G | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-30-2827T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026866 | ||||||
chr2:201026983
|
T | C | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30-2944A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201026983 | ||||||
chr2:201027014
|
T | G | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-2975A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027014 | ||||||
chr2:201027029
|
G | T | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-30-2990C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027029 | ||||||
chr2:201027070
|
G | A | 8 | a0001c0001t0004g0105a0001c0001t0005g0152a0001c0001t0005g0153others(5): Show | 8 | HG02080.hp1 HG02083.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-3031C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027070 | ||||||
chr2:201027197
|
T | G | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-30-3158A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027197 | ||||||
chr2:201027279
|
C | T | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-30-3240G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027279 | ||||||
chr2:201027409
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30-3370A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027409 | ||||||
chr2:201027465
|
G | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-3426C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027465 | ||||||
chr2:201027553
|
C | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-30-3514G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027553 | ||||||
chr2:201027577
|
C | T | 1 | a0001c0001t0004g0089 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-30-3538G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027577 | ||||||
chr2:201027766
|
C | G | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-30-3727G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027766 | ||||||
chr2:201027792
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3753G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027792 | ||||||
chr2:201027796
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3757C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027796 | ||||||
chr2:201027799
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3760A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027799 | ||||||
chr2:201027812
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3773T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027812 | ||||||
chr2:201027826
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3787G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027826 | ||||||
chr2:201027833
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3794A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027833 | ||||||
chr2:201027844
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-30-3805A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027844 | ||||||
chr2:201027946
|
G | A | 1 | a0001c0001t0020g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-30-3907C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027946 | ||||||
chr2:201027948
|
TG | T | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-3910delC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027948 | ||||||
chr2:201027969
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-30-3930A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027969 | ||||||
chr2:201027993
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-30-3954C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201027993 | ||||||
chr2:201028076
|
G | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-4037C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028076 | ||||||
chr2:201028109
|
C | G | 1 | a0001c0001t0043g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-30-4070G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028109 | ||||||
chr2:201028137
|
G | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-4098C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028137 | ||||||
chr2:201028228
|
G | C | 1 | a0001c0001t0020g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-30-4189C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028228 | ||||||
chr2:201028357
|
G | C | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-4318C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028357 | ||||||
chr2:201028436
|
T | C | 1 | a0001c0001t0004g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-30-4397A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028436 | ||||||
chr2:201028465
|
T | C | 78 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-30-4426A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028465 | ||||||
chr2:201028537
|
G | A | 1 | a0001c0001t0003g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-30-4498C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028537 | ||||||
chr2:201028611
|
C | G | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30-4572G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028611 | ||||||
chr2:201028636
|
A | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-4597T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028636 | ||||||
chr2:201028693
|
G | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-4654C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028693 | ||||||
chr2:201028709
|
G | A | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-4670C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028709 | ||||||
chr2:201028742
|
G | A | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-30-4703C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028742 | ||||||
chr2:201028882
|
A | G | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-30-4843T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028882 | ||||||
chr2:201028902
|
G | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-30-4863C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201028902 | ||||||
chr2:201029139
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-30-5100C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029139 | ||||||
chr2:201029152
|
G | T | 1 | a0001c0001t0043g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-30-5113C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029152 | ||||||
chr2:201029191
|
C | A | 6 | a0001c0001t0008g0002a0001c0001t0008g0111a0001c0001t0008g0115others(3): Show | 7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-5152G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029191 | ||||||
chr2:201029296
|
A | G | 70 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(67): Show | 72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-5257T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029296 | ||||||
chr2:201029735
|
C | G | 1 | a0001c0001t0033g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-30-5696G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029735 | ||||||
chr2:201029851
|
G | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-30-5812C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029851 | ||||||
chr2:201029963
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0021g0174a0001c0001t0037g0083 | 3 | HG00099.hp1 HG02080.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-30-5924C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201029963 | ||||||
chr2:201030094
|
A | G | 1 | a0001c0001t0011g0170 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-30-6055T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030094 | ||||||
chr2:201030107
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-30-6068G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030107 | ||||||
chr2:201030220
|
A | T | 78 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-30-6181T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030220 | ||||||
chr2:201030315
|
T | A | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30-6276A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030315 | ||||||
chr2:201030570
|
T | G | 6 | a0001c0001t0008g0002a0001c0001t0008g0111a0001c0001t0008g0115others(3): Show | 7 | HG01109.hp2 HG01243.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-6531A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030570 | ||||||
chr2:201030582
|
C | CT | 21 | a0001c0001t0001g0043a0001c0001t0002g0015a0001c0001t0002g0016others(18): Show | 21 | HG00099.hp2 HG00408.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30-6544dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030582 | ||||||
chr2:201030586
|
T | C | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30-6547A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030586 | ||||||
chr2:201030760
|
G | A | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-6721C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201030760 | ||||||
chr2:201031025
|
GTGT | G | 2 | a0001c0001t0004g0105a0001c0001t0029g0123 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-30-6989_-30-6987d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031025 | ||||||
chr2:201031344
|
A | G | 2 | a0001c0001t0009g0032a0001c0001t0009g0048 | 2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-30-7305T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031344 | ||||||
chr2:201031592
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-7553C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031592 | ||||||
chr2:201031644
|
T | C | 70 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(67): Show | 72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-30-7605A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031644 | ||||||
chr2:201031843
|
T | C | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-7804A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201031843 | ||||||
chr2:201032086
|
G | A | 2 | a0001c0001t0008g0142a0001c0001t0035g0143 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-8047C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201032086 | ||||||
chr2:201033145
|
TTGTA | T | 2 | a0001c0001t0008g0142a0001c0001t0035g0143 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-30-9110_-30-9107d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033145 | ||||||
chr2:201033149
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0134 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-30-9126_-30-9111d others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033149 | ||||||
chr2:201033155
|
GTGTA | G | 2 | a0001c0001t0003g0163a0001c0001t0012g0092 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-30-9120_-30-9117d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033155 | ||||||
chr2:201033157
|
GTA | G | 10 | a0001c0001t0003g0128a0001c0001t0003g0129a0001c0001t0003g0133others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-9120_-30-9119d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033157 | ||||||
chr2:201033159
|
A | ATG | 15 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0001g0173others(12): Show | 15 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-30-9122_-30-9121d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | ||||||
chr2:201033159
|
A | ATGTG | 9 | a0001c0001t0001g0055a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 9 | HG00558.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9124_-30-9121d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | ||||||
chr2:201033159
|
A | G | 45 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.-30-9120T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | ||||||
chr2:201033159
|
ATG | A | 12 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG00741.hp1 HG01243.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-9122_-30-9121d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | ||||||
chr2:201033159
|
ATGTG | A | 9 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0093others(6): Show | 9 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9124_-30-9121d others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033159 | ||||||
chr2:201033188
|
T | A | 1 | a0001c0001t0003g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-30-9149A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033188 | ||||||
chr2:201033190
|
T | A | 15 | a0001c0001t0003g0134a0001c0001t0003g0163a0001c0001t0004g0105others(12): Show | 16 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-30-9151A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033190 | ||||||
chr2:201033190
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-30-9161_-30-9152d others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033190 | ||||||
chr2:201033192
|
T | A | 47 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0128others(44): Show | 49 | HG00642.hp1 HG00733.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.-30-9153A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033192 | ||||||
chr2:201033192
|
T | TGA | 3 | a0001c0001t0006g0108a0001c0001t0006g0119a0001c0001t0024g0166 | 3 | HG00280.hp2 HG01168.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30-9154_-30-9153i others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033192 | ||||||
chr2:201033194
|
T | A | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-30-9155A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033194 | ||||||
chr2:201033194
|
T | TGAGA | 2 | a0001c0001t0034g0172a0001c0001t0041g0160 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-30-9156_-30-9155i others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033194 | ||||||
chr2:201033196
|
T | A | 60 | a0001c0001t0001g0038a0001c0001t0002g0158a0001c0001t0003g0120others(57): Show | 62 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30-9157A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033196
|
T | TGA | 2 | a0001c0001t0005g0019a0001c0001t0005g0154 | 2 | NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-30-9159_-30-9158d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033196
|
T | TGTGA | 9 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0152others(6): Show | 9 | HG01071.hp2 HG02615.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033196
|
T | TGTGTGAG others(1): Show |
2 | a0001c0001t0007g0077a0001c0001t0042g0060 | 2 | HG00140.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033196
|
T | TGTGTGTG others(1): Show |
2 | a0001c0001t0002g0021a0001c0001t0003g0036 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-9158_-30-9157i others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033196
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0002g0020 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-30-9158_-30-9157i others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033196 | ||||||
chr2:201033198
|
A | T | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG01952.hp2 HG02615.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-9159T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033198 | ||||||
chr2:201033200
|
A | T | 2 | a0001c0001t0014g0139a0001c0001t0014g0141 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-30-9161T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033200 | ||||||
chr2:201033243
|
C | T | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-9204G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033243 | ||||||
chr2:201033339
|
G | C | 9 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30-9300C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033339 | ||||||
chr2:201033371
|
A | ATTTAT | 11 | a0001c0001t0001g0042a0001c0001t0001g0065a0001c0001t0001g0095others(8): Show | 11 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-9337_-30-9333d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | ||||||
chr2:201033371
|
ATTTAT | A | 26 | a0001c0001t0001g0051a0001c0001t0002g0158a0001c0001t0003g0127others(23): Show | 26 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30-9337_-30-9333d others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | ||||||
chr2:201033371
|
ATTTATTT others(3): Show |
A | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-30-9342_-30-9333d others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033371 | ||||||
chr2:201033504
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30-9465G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033504 | ||||||
chr2:201033505
|
G | A | 4 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(1): Show | 4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-9466C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033505 | ||||||
chr2:201033704
|
C | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-9665G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033704 | ||||||
chr2:201033722
|
A | AT | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-30-9684dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033722 | ||||||
chr2:201033731
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-30-9692C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033731 | ||||||
chr2:201033913
|
T | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-30-9874A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033913 | ||||||
chr2:201033925
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-30-9886A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201033925 | ||||||
chr2:201034162
|
A | ACAT | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-10126_-30-1012 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034162 | ||||||
chr2:201034415
|
A | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-30-10376T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034415 | ||||||
chr2:201034477
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30-10438G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034477 | ||||||
chr2:201034562
|
T | C | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-30-10523A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034562 | ||||||
chr2:201034801
|
G | C | 1 | a0001c0001t0008g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+10695C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034801 | ||||||
chr2:201034826
|
C | T | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-31+10670G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201034826 | ||||||
chr2:201035115
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+10381C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035115 | ||||||
chr2:201035166
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-31+10330T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035166 | ||||||
chr2:201035226
|
C | T | 3 | a0001c0001t0004g0089a0001c0001t0004g0125a0001c0001t0033g0126 | 3 | HG00733.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-31+10270G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035226 | ||||||
chr2:201035293
|
G | C | 1 | a0001c0001t0006g0119 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-31+10203C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035293 | ||||||
chr2:201035296
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+10200G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035296 | ||||||
chr2:201035300
|
T | A | 1 | a0001c0001t0009g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-31+10196A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035300 | ||||||
chr2:201035407
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+10089A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035407 | ||||||
chr2:201035417
|
G | A | 14 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0090others(11): Show | 15 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-31+10079C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035417 | ||||||
chr2:201035763
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-31+9733G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035763 | ||||||
chr2:201035798
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-31+9698C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035798 | ||||||
chr2:201035851
|
G | C | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+9645C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201035851 | ||||||
chr2:201036067
|
A | G | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-31+9429T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036067 | ||||||
chr2:201036447
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-31+9049T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036447 | ||||||
chr2:201036466
|
C | G | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+9030G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036466 | ||||||
chr2:201036513
|
C | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+8983G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036513 | ||||||
chr2:201036697
|
C | G | 1 | a0001c0001t0032g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-31+8799G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036697 | ||||||
chr2:201036948
|
G | A | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+8548C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201036948 | ||||||
chr2:201037194
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+8302C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037194 | ||||||
chr2:201037251
|
A | C | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+8245T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037251 | ||||||
chr2:201037543
|
G | C | 1 | a0001c0001t0004g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-31+7953C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037543 | ||||||
chr2:201037621
|
G | C | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+7875C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037621 | ||||||
chr2:201037650
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+7846A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037650 | ||||||
chr2:201037827
|
C | T | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+7669G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037827 | ||||||
chr2:201037938
|
C | T | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7558G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037938 | ||||||
chr2:201037939
|
A | G | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7557T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037939 | ||||||
chr2:201037988
|
T | A | 70 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(67): Show | 72 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-31+7508A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201037988 | ||||||
chr2:201038074
|
T | C | 1 | a0001c0001t0010g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+7422A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038074 | ||||||
chr2:201038083
|
A | C | 1 | a0001c0001t0010g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-31+7413T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038083 | ||||||
chr2:201038553
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-31+6943G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038553 | ||||||
chr2:201038561
|
C | T | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+6935G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038561 | ||||||
chr2:201038618
|
T | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+6878A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038618 | ||||||
chr2:201038845
|
G | A | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31+6651C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038845 | ||||||
chr2:201038913
|
T | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6583A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038913 | ||||||
chr2:201038928
|
TA | T | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+6567delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201038928 | ||||||
chr2:201039104
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-31+6392G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039104 | ||||||
chr2:201039216
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+6280G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039216 | ||||||
chr2:201039410
|
T | G | 1 | a0001c0001t0008g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-31+6086A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039410 | ||||||
chr2:201039578
|
C | T | 78 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-31+5918G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039578 | ||||||
chr2:201039723
|
G | A | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-31+5773C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039723 | ||||||
chr2:201039736
|
C | T | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+5760G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039736 | ||||||
chr2:201039742
|
G | A | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+5754C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039742 | ||||||
chr2:201039743
|
T | C | 83 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(80): Show | 85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-31+5753A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039743 | ||||||
chr2:201039971
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-31+5525C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201039971 | ||||||
chr2:201040002
|
G | A | 1 | a0001c0001t0004g0125 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-31+5494C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040002 | ||||||
chr2:201040130
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0085 | 2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-31+5366C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040130 | ||||||
chr2:201040441
|
T | TTTG | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+5052_-31+5054d others(5): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040441 | ||||||
chr2:201040459
|
G | GT | 6 | a0001c0001t0001g0022a0001c0001t0004g0121a0001c0001t0004g0124others(3): Show | 6 | HG00280.hp2 HG01175.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+5036dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040459 | ||||||
chr2:201040459
|
G | T | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-31+5037C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040459 | ||||||
chr2:201040462
|
T | G | 1 | a0001c0001t0011g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-31+5034A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040462 | ||||||
chr2:201040646
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+4850C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040646 | ||||||
chr2:201040765
|
G | A | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-31+4731C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040765 | ||||||
chr2:201040941
|
A | G | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+4555T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040941 | ||||||
chr2:201040996
|
T | TAAACCCT others(24): Show |
1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31+4469_-31+4499d others(33): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201040996 | ||||||
chr2:201041139
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-31+4357T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041139 | ||||||
chr2:201041366
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-31+4130G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041366 | ||||||
chr2:201041792
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-31+3704T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041792 | ||||||
chr2:201041845
|
T | C | 1 | a0001c0001t0010g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+3651A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041845 | ||||||
chr2:201041938
|
T | C | 83 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(80): Show | 85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-31+3558A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201041938 | ||||||
chr2:201042005
|
G | C | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-31+3491C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042005 | ||||||
chr2:201042046
|
C | T | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-31+3450G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042046 | ||||||
chr2:201042073
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-31+3423G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042073 | ||||||
chr2:201042089
|
T | C | 2 | a0001c0001t0003g0161a0001c0001t0003g0165 | 2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-31+3407A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042089 | ||||||
chr2:201042102
|
A | C | 1 | a0001c0001t0003g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-31+3394T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042102 | ||||||
chr2:201042158
|
G | T | 1 | a0001c0001t0017g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-31+3338C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042158 | ||||||
chr2:201042301
|
C | T | 1 | a0001c0001t0007g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-31+3195G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042301 | ||||||
chr2:201042532
|
A | AC | 16 | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0001g0051others(13): Show | 16 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+2963dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042532 | ||||||
chr2:201042598
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+2898C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042598 | ||||||
chr2:201042632
|
G | A | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-31+2864C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042632 | ||||||
chr2:201042664
|
G | C | 1 | a0001c0001t0045g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-31+2832C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042664 | ||||||
chr2:201042692
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+2804C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042692 | ||||||
chr2:201042741
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2755C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042741 | ||||||
chr2:201042755
|
G | A | 6 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG02109.hp1 HG02486.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+2741C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042755 | ||||||
chr2:201042839
|
A | AC | 9 | a0001c0001t0001g0022a0001c0001t0001g0068a0001c0001t0001g0076others(6): Show | 9 | HG01175.hp2 HG01433.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+2656dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042839 | ||||||
chr2:201042854
|
T | TG | 25 | a0001c0001t0001g0043a0001c0001t0002g0158a0001c0001t0003g0127others(22): Show | 25 | HG00408.hp2 HG01192.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-31+2641dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042854 | ||||||
chr2:201042910
|
G | A | 10 | a0001c0001t0001g0051a0001c0001t0005g0019a0001c0001t0005g0147others(7): Show | 10 | HG01243.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-31+2586C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042910 | ||||||
chr2:201042917
|
A | AC | 20 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0001g0042others(17): Show | 20 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-31+2578dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201042917 | ||||||
chr2:201043041
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2455A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043041 | ||||||
chr2:201043191
|
G | C | 1 | a0001c0001t0004g0121 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-31+2305C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043191 | ||||||
chr2:201043432
|
T | TA | 7 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0051others(4): Show | 7 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+2063dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043432 | ||||||
chr2:201043432
|
T | TAA | 10 | a0001c0001t0005g0019a0001c0001t0005g0148a0001c0001t0005g0152others(7): Show | 10 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31+2062_-31+2063d others(4): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043432 | ||||||
chr2:201043434
|
A | T | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-31+2062T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043434 | ||||||
chr2:201043446
|
A | G | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-31+2050T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043446 | ||||||
chr2:201043447
|
A | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-31+2049T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043447 | ||||||
chr2:201043450
|
G | A | 3 | a0001c0001t0004g0110a0001c0001t0008g0142a0001c0001t0035g0143 | 3 | HG00642.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-31+2046C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043450 | ||||||
chr2:201043466
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-31+2030T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043466 | ||||||
chr2:201043569
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+1927G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043569 | ||||||
chr2:201043638
|
A | G | 18 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0090others(15): Show | 19 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-31+1858T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043638 | ||||||
chr2:201043814
|
G | A | 74 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(71): Show | 76 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-31+1682C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201043814 | ||||||
chr2:201044335
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+1161C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044335 | ||||||
chr2:201044425
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-31+1071T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044425 | ||||||
chr2:201044556
|
G | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+940C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044556 | ||||||
chr2:201044670
|
C | T | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-31+826G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044670 | ||||||
chr2:201044792
|
A | G | 29 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(26): Show |
intron_variant | MODIFIER | c.-31+704T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044792 | ||||||
chr2:201044847
|
C | T | 1 | a0001c0001t0010g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-31+649G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044847 | ||||||
chr2:201044971
|
A | G | 1 | a0001c0001t0037g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-31+525T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201044971 | ||||||
chr2:201045172
|
C | T | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-31+324G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045172 | ||||||
chr2:201045173
|
G | A | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-31+323C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045173 | ||||||
chr2:201045305
|
A | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+191T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045305 | ||||||
chr2:201045480
|
A | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-31+16T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 2/12 | chr2 | 201045480 | ||||||
chr2:201045607
|
A | G | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-128-14T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045607 | ||||||
chr2:201045665
|
T | C | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-128-72A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045665 | ||||||
chr2:201045936
|
T | C | 9 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-343A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201045936 | ||||||
chr2:201046006
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-128-413G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046006 | ||||||
chr2:201046118
|
A | G | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-525T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046118 | ||||||
chr2:201046235
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-128-642A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046235 | ||||||
chr2:201046239
|
A | G | 1 | a0001c0001t0002g0070 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-128-646T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046239 | ||||||
chr2:201046371
|
T | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-778A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046371 | ||||||
chr2:201046424
|
G | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-831C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046424 | ||||||
chr2:201046426
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-833C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046426 | ||||||
chr2:201046441
|
A | G | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-848T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046441 | ||||||
chr2:201046719
|
G | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-1126C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046719 | ||||||
chr2:201046903
|
A | T | 1 | a0001c0001t0023g0137 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-128-1310T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046903 | ||||||
chr2:201046987
|
T | C | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-1394A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201046987 | ||||||
chr2:201047199
|
A | G | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-1606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047199 | ||||||
chr2:201047268
|
G | T | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-128-1675C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047268 | ||||||
chr2:201047445
|
C | CAT | 5 | a0001c0001t0001g0042a0001c0001t0002g0069a0001c0001t0008g0142others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-1854_-128-185 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATAT | 2 | a0001c0001t0004g0110a0001c0001t0019g0018 | 2 | HG00642.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-128-1856_-128-185 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(1): Show |
11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02717.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-128-1860_-128-185 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(3): Show |
4 | a0001c0001t0002g0158a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02647.hp1 HG02895.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-1862_-128-185 others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(5): Show |
23 | a0001c0001t0003g0120a0001c0001t0003g0131a0001c0001t0004g0001others(20): Show | 25 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-128-1864_-128-185 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(7): Show |
12 | a0001c0001t0003g0127a0001c0001t0003g0129a0001c0001t0003g0133others(9): Show | 12 | HG00733.hp1 HG01515.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.-128-1866_-128-185 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(9): Show |
3 | a0001c0001t0003g0128a0001c0001t0004g0117a0001c0001t0008g0111 | 3 | HG02451.hp2 HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-128-1868_-128-185 others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(11): Show |
1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-128-1870_-128-185 others(22): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(13): Show |
5 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0004g0105others(2): Show | 5 | HG02083.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-1872_-128-185 others(24): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(15): Show |
4 | a0001c0001t0003g0161a0001c0001t0011g0167a0001c0001t0011g0168others(1): Show | 4 | HG02630.hp1 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-128-1853_-128-185 others(26): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(17): Show |
2 | a0001c0001t0011g0159a0001c0001t0024g0166 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-128-1853_-128-185 others(28): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
C | CATATATA others(19): Show |
1 | a0001c0001t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-128-1853_-128-185 others(30): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047445
|
CAT | C | 2 | a0001c0001t0028g0144a0001c0001t0044g0096 | 2 | HG02145.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.-128-1854_-128-185 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047445 | ||||||
chr2:201047465
|
T | TATATATA others(7): Show |
1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-128-1873_-128-187 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047465 | ||||||
chr2:201047559
|
G | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-1966C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047559 | ||||||
chr2:201047680
|
A | G | 1 | a0001c0001t0028g0144 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-128-2087T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047680 | ||||||
chr2:201047795
|
ACTGTTAA others(5): Show |
A | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0051others(2): Show | 5 | HG00642.hp2 HG01243.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-2214_-128-220 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047795 | ||||||
chr2:201047890
|
C | CA | 40 | a0001c0001t0001g0072a0001c0001t0002g0158a0001c0001t0003g0127others(37): Show | 41 | HG00099.hp1 HG00741.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.-128-2298dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047890 | ||||||
chr2:201047890
|
C | CAA | 8 | a0001c0001t0001g0022a0001c0001t0002g0020a0001c0001t0002g0021others(5): Show | 8 | HG01175.hp2 HG02280.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-2299_-128-229 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201047890 | ||||||
chr2:201048506
|
A | AT | 61 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(58): Show | 63 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-128-2914dupA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048506 | ||||||
chr2:201048506
|
A | ATTT | 6 | a0001c0001t0005g0147a0001c0001t0005g0152a0001c0001t0005g0153others(3): Show | 6 | HG02886.hp1 HG02897.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-128-2916_-128-291 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048506 | ||||||
chr2:201048522
|
A | T | 78 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-128-2929T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048522 | ||||||
chr2:201048542
|
G | A | 4 | a0001c0001t0002g0086a0001c0001t0005g0155a0001c0001t0005g0156others(1): Show | 4 | HG00099.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-2949C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048542 | ||||||
chr2:201048561
|
A | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-2968T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048561 | ||||||
chr2:201048706
|
C | G | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-3113G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048706 | ||||||
chr2:201048859
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-3266G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201048859 | ||||||
chr2:201049199
|
A | G | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-128-3606T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049199 | ||||||
chr2:201049389
|
G | A | 1 | a0001c0001t0004g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-3796C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049389 | ||||||
chr2:201049510
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-3917G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049510 | ||||||
chr2:201049517
|
T | G | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-3924A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049517 | ||||||
chr2:201049587
|
T | C | 1 | a0001c0001t0002g0008 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-128-3994A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049587 | ||||||
chr2:201049642
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0015g0006 | 3 | HG01192.hp1 HG01257.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-128-4049G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049642 | ||||||
chr2:201049658
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-128-4065A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049658 | ||||||
chr2:201049891
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-128-4298G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201049891 | ||||||
chr2:201050110
|
C | G | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-4517G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050110 | ||||||
chr2:201050122
|
G | A | 6 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(3): Show | 6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-4529C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050122 | ||||||
chr2:201050159
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-4566T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050159 | ||||||
chr2:201050212
|
T | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-4619A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050212 | ||||||
chr2:201050213
|
CA | C | 6 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(3): Show | 6 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-128-4621delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050213 | ||||||
chr2:201050599
|
GA | G | 6 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(3): Show | 6 | HG02486.hp1 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-5007delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050599 | ||||||
chr2:201050607
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-128-5014T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050607 | ||||||
chr2:201050628
|
C | G | 1 | a0001c0001t0042g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-128-5035G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050628 | ||||||
chr2:201050759
|
A | AC | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-5167dupG | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201050759 | ||||||
chr2:201051085
|
T | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-5492A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051085 | ||||||
chr2:201051322
|
A | G | 6 | a0001c0001t0011g0159a0001c0001t0011g0167a0001c0001t0011g0168others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-128-5729T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051322 | ||||||
chr2:201051352
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0065 | 3 | HG01496.hp1 HG01515.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-128-5759C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051352 | ||||||
chr2:201051695
|
G | C | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-6102C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201051695 | ||||||
chr2:201052105
|
T | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-6512A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052105 | ||||||
chr2:201052246
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-6653C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052246 | ||||||
chr2:201052276
|
A | G | 3 | a0001c0001t0011g0167a0001c0001t0011g0168a0001c0001t0040g0164 | 3 | HG02622.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-128-6683T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052276 | ||||||
chr2:201052285
|
G | A | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-128-6692C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052285 | ||||||
chr2:201052354
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-128-6761G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052354 | ||||||
chr2:201052443
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-128-6850T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052443 | ||||||
chr2:201052900
|
G | C | 5 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(2): Show | 5 | HG02486.hp1 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-128-7307C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201052900 | ||||||
chr2:201053019
|
A | G | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-7426T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053019 | ||||||
chr2:201053209
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-7616C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053209 | ||||||
chr2:201053215
|
T | C | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-128-7622A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053215 | ||||||
chr2:201053236
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-128-7643G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053236 | ||||||
chr2:201053416
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-7823T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053416 | ||||||
chr2:201053505
|
C | G | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-128-7912G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053505 | ||||||
chr2:201053612
|
G | A | 2 | a0001c0001t0004g0105a0001c0001t0029g0123 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-128-8019C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053612 | ||||||
chr2:201053736
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-128-8143C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053736 | ||||||
chr2:201053882
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-8289A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201053882 | ||||||
chr2:201054083
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-8490G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054083 | ||||||
chr2:201054096
|
T | G | 3 | a0001c0001t0001g0173a0001c0001t0002g0088a0001c0001t0002g0099 | 3 | HG03491.hp1 NA18963.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-128-8503A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054096 | ||||||
chr2:201054122
|
C | G | 1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-128-8529G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054122 | ||||||
chr2:201054289
|
T | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0007g0100 | 3 | HG01069.hp1 HG01192.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-128-8696A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054289 | ||||||
chr2:201054498
|
T | A | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-8905A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054498 | ||||||
chr2:201054629
|
C | G | 1 | a0001c0001t0004g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-128-9036G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054629 | ||||||
chr2:201054825
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-9232C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201054825 | ||||||
chr2:201055042
|
T | C | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-9449A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055042 | ||||||
chr2:201055243
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-9650G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055243 | ||||||
chr2:201055337
|
G | A | 51 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(48): Show | 53 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-128-9744C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055337 | ||||||
chr2:201055383
|
G | GA | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-128-9791dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055383 | ||||||
chr2:201055384
|
A | G | 2 | a0001c0001t0027g0033a0001c0001t0031g0091 | 2 | HG02109.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-128-9791T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055384 | ||||||
chr2:201055493
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-128-9900C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055493 | ||||||
chr2:201055494
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-128-9901A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055494 | ||||||
chr2:201055500
|
A | T | 3 | a0001c0001t0004g0089a0001c0001t0004g0125a0001c0001t0033g0126 | 3 | HG00733.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-128-9907T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055500 | ||||||
chr2:201055555
|
A | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-9962T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055555 | ||||||
chr2:201055895
|
T | C | 31 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0089others(28): Show | 33 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-128-10302A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201055895 | ||||||
chr2:201056016
|
G | A | 4 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(1): Show | 4 | HG01261.hp1 HG03491.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-128-10423C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056016 | ||||||
chr2:201056060
|
G | T | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-128-10467C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056060 | ||||||
chr2:201056121
|
G | T | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-10528C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056121 | ||||||
chr2:201056143
|
G | A | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-128-10550C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056143 | ||||||
chr2:201056151
|
G | A | 1 | a0001c0001t0013g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-128-10558C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056151 | ||||||
chr2:201056175
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-128-10582C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056175 | ||||||
chr2:201056188
|
C | A | 9 | a0001c0001t0003g0127a0001c0001t0003g0128a0001c0001t0003g0129others(6): Show | 9 | HG02055.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-10595G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056188 | ||||||
chr2:201056201
|
A | T | 14 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(11): Show | 14 | HG02280.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-128-10608T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056201 | ||||||
chr2:201056204
|
A | AAATAAAT others(4): Show |
2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-10612_-128-10 others(17): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056204 | ||||||
chr2:201056205
|
T | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-128-10612A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056205 | ||||||
chr2:201056205
|
T | TAAATAAA others(2): Show |
11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-128-10613_-128-10 others(15): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056205 | ||||||
chr2:201056535
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-10942C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056535 | ||||||
chr2:201056606
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-128-11013C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056606 | ||||||
chr2:201056674
|
C | CA | 10 | a0001c0001t0005g0019a0001c0001t0013g0003a0001c0001t0013g0005others(7): Show | 10 | HG00741.hp1 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-128-11082dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056674 | ||||||
chr2:201056718
|
T | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-11125A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056718 | ||||||
chr2:201056739
|
T | C | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-128-11146A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201056739 | ||||||
chr2:201057010
|
G | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-128-11417C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057010 | ||||||
chr2:201057198
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-128-11605T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057198 | ||||||
chr2:201057874
|
A | C | 1 | a0001c0001t0026g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-128-12281T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201057874 | ||||||
chr2:201058008
|
C | T | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-12415G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058008 | ||||||
chr2:201058014
|
T | C | 1 | a0001c0001t0003g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-128-12421A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058014 | ||||||
chr2:201058262
|
A | G | 1 | a0001c0001t0008g0116 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-128-12669T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058262 | ||||||
chr2:201058298
|
A | C | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-128-12705T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058298 | ||||||
chr2:201058411
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-128-12818A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058411 | ||||||
chr2:201058434
|
A | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-128-12841T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058434 | ||||||
chr2:201058568
|
G | A | 2 | a0001c0001t0016g0014a0001c0001t0016g0074 | 2 | NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-128-12975C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058568 | ||||||
chr2:201058599
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-128-13006C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058599 | ||||||
chr2:201058621
|
C | A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129+12989G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058621 | ||||||
chr2:201058759
|
C | G | 8 | a0001c0001t0001g0038a0001c0001t0001g0066a0001c0001t0001g0067others(5): Show | 8 | HG00733.hp2 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-129+12851G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058759 | ||||||
chr2:201058912
|
C | T | 17 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(14): Show | 17 | HG02280.hp1 HG02615.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-129+12698G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201058912 | ||||||
chr2:201059200
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+12410G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059200 | ||||||
chr2:201059231
|
T | C | 1 | a0001c0001t0004g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-129+12379A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059231 | ||||||
chr2:201059335
|
T | C | 2 | a0001c0001t0034g0172a0001c0001t0040g0164 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-129+12275A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059335 | ||||||
chr2:201059355
|
C | T | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-129+12255G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059355 | ||||||
chr2:201059635
|
G | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11975C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059635 | ||||||
chr2:201059726
|
G | C | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11884C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059726 | ||||||
chr2:201059765
|
A | G | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11845T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059765 | ||||||
chr2:201059792
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+11818A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059792 | ||||||
chr2:201059876
|
T | A | 3 | a0001c0001t0009g0032a0001c0001t0009g0048a0001c0001t0009g0049 | 3 | HG02809.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-129+11734A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059876 | ||||||
chr2:201059905
|
C | T | 4 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-129+11705G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201059905 | ||||||
chr2:201060009
|
T | A | 124 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 126 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-129+11601A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060009 | ||||||
chr2:201060054
|
C | CG | 40 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(37): Show | 40 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-129+11555dupC | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | ||||||
chr2:201060054
|
C | CGG | 16 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0075others(13): Show | 16 | HG00140.hp1 HG01192.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.-129+11554_-129+11 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | ||||||
chr2:201060054
|
CGG | C | 18 | a0001c0001t0002g0158a0001c0001t0003g0128a0001c0001t0003g0129others(15): Show | 18 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-129+11554_-129+11 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060054 | ||||||
chr2:201060059
|
G | C | 1 | a0001c0001t0004g0125 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-129+11551C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060059 | ||||||
chr2:201060060
|
G | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+11550C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060060 | ||||||
chr2:201060065
|
G | C | 2 | a0001c0001t0003g0165a0001c0001t0014g0141 | 2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-129+11545C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | ||||||
chr2:201060065
|
G | GT | 4 | a0001c0001t0004g0105a0001c0001t0006g0104a0001c0001t0008g0115others(1): Show | 4 | HG02027.hp2 HG02083.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-129+11544_-129+11 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | ||||||
chr2:201060065
|
G | T | 27 | a0001c0001t0003g0120a0001c0001t0004g0001a0001c0001t0004g0089others(24): Show | 29 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.-129+11545C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060065 | ||||||
chr2:201060066
|
G | C | 9 | a0001c0001t0005g0147a0001c0001t0005g0148a0001c0001t0005g0152others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+11544C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060066 | ||||||
chr2:201060066
|
G | GC | 2 | a0001c0001t0005g0019a0002c0002t0005g0151 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-129+11543_-129+11 others(7): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060066 | ||||||
chr2:201060101
|
G | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+11509C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060101 | ||||||
chr2:201060210
|
G | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+11400C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060210 | ||||||
chr2:201060562
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+11048A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060562 | ||||||
chr2:201060619
|
T | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+10991A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060619 | ||||||
chr2:201060738
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+10872T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201060738 | ||||||
chr2:201061072
|
CA | C | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02109.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+10537delT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061072 | ||||||
chr2:201061078
|
A | C | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+10532T>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061078 | ||||||
chr2:201061092
|
T | C | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+10518A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061092 | ||||||
chr2:201061127
|
G | C | 1 | a0001c0001t0024g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-129+10483C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061127 | ||||||
chr2:201061627
|
GT | G | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG01069.hp2 HG01071.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+9982delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061627 | ||||||
chr2:201061635
|
T | A | 1 | a0001c0001t0007g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-129+9975A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061635 | ||||||
chr2:201061641
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-129+9969T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201061641 | ||||||
chr2:201062115
|
A | G | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+9495T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062115 | ||||||
chr2:201062377
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+9233C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062377 | ||||||
chr2:201062524
|
A | G | 165 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-129+9086T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062524 | ||||||
chr2:201062591
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+9019G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062591 | ||||||
chr2:201062646
|
G | C | 1 | a0001c0001t0033g0126 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-129+8964C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201062646 | ||||||
chr2:201063119
|
G | A | 22 | a0001c0001t0002g0158a0001c0001t0003g0127a0001c0001t0003g0128others(19): Show | 22 | HG02055.hp1 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-129+8491C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063119 | ||||||
chr2:201063170
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-129+8440C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063170 | ||||||
chr2:201063197
|
C | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+8413G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063197 | ||||||
chr2:201063198
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-129+8412C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063198 | ||||||
chr2:201063266
|
G | A | 1 | a0001c0001t0045g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-129+8344C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063266 | ||||||
chr2:201063360
|
C | T | 53 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(50): Show | 55 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.-129+8250G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063360 | ||||||
chr2:201063563
|
G | A | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+8047C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063563 | ||||||
chr2:201063762
|
A | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-129+7848T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063762 | ||||||
chr2:201063878
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-129+7732C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063878 | ||||||
chr2:201063886
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-129+7724G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063886 | ||||||
chr2:201063948
|
G | T | 2 | a0001c0001t0021g0174a0001c0001t0034g0172 | 2 | HG02280.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-129+7662C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201063948 | ||||||
chr2:201064003
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-129+7607A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064003 | ||||||
chr2:201064308
|
AT | A | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+7301delA | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064308 | ||||||
chr2:201064395
|
G | T | 3 | a0001c0001t0014g0139a0001c0001t0014g0140a0001c0001t0014g0141 | 3 | HG02615.hp1 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-129+7215C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064395 | ||||||
chr2:201064483
|
T | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+7127A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064483 | ||||||
chr2:201064496
|
T | C | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+7114A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064496 | ||||||
chr2:201064530
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG00738.hp1 HG01257.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-129+7080C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064530 | ||||||
chr2:201064530
|
G | C | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+7080C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064530 | ||||||
chr2:201064909
|
T | C | 6 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(3): Show | 6 | HG01261.hp1 HG02145.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+6701A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064909 | ||||||
chr2:201064945
|
T | C | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+6665A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064945 | ||||||
chr2:201064974
|
C | G | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+6636G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201064974 | ||||||
chr2:201065043
|
G | T | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+6567C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065043 | ||||||
chr2:201065338
|
T | C | 1 | a0001c0001t0007g0045 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-129+6272A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065338 | ||||||
chr2:201065521
|
G | A | 8 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(5): Show | 8 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+6089C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065521 | ||||||
chr2:201065957
|
C | T | 1 | a0001c0001t0012g0092 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-129+5653G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201065957 | ||||||
chr2:201066019
|
A | T | 1 | a0001c0001t0016g0074 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-129+5591T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066019 | ||||||
chr2:201066085
|
T | G | 1 | a0001c0001t0010g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-129+5525A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066085 | ||||||
chr2:201066100
|
CAG | C | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+5508_-129+550 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066100 | ||||||
chr2:201066207
|
A | G | 78 | a0001c0001t0002g0158a0001c0001t0003g0120a0001c0001t0003g0127others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.-129+5403T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066207 | ||||||
chr2:201066669
|
T | C | 1 | a0001c0001t0024g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-129+4941A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066669 | ||||||
chr2:201066698
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+4912G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066698 | ||||||
chr2:201066699
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+4911C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066699 | ||||||
chr2:201066856
|
C | T | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+4754G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066856 | ||||||
chr2:201066887
|
T | C | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+4723A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201066887 | ||||||
chr2:201067007
|
T | C | 83 | a0001c0001t0001g0157a0001c0001t0002g0020a0001c0001t0002g0021others(80): Show | 85 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.-129+4603A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067007 | ||||||
chr2:201067201
|
G | T | 9 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(6): Show | 9 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-129+4409C>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067201 | ||||||
chr2:201067233
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+4377G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067233 | ||||||
chr2:201067385
|
T | C | 1 | a0001c0001t0005g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-129+4225A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201067385 | ||||||
chr2:201068050
|
C | T | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-129+3560G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068050 | ||||||
chr2:201068075
|
C | T | 1 | a0001c0001t0031g0091 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-129+3535G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068075 | ||||||
chr2:201068076
|
G | A | 1 | a0001c0001t0019g0018 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-129+3534C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068076 | ||||||
chr2:201068211
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+3399G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068211 | ||||||
chr2:201068244
|
G | A | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+3366C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068244 | ||||||
chr2:201068347
|
C | T | 2 | a0001c0001t0017g0149a0001c0001t0017g0150 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-129+3263G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068347 | ||||||
chr2:201068398
|
G | A | 13 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+3212C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068398 | ||||||
chr2:201068487
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0003g0036 | 3 | HG02896.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-129+3123G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068487 | ||||||
chr2:201068920
|
C | CA | 6 | a0001c0001t0009g0032a0001c0001t0009g0046a0001c0001t0009g0048others(3): Show | 6 | HG02647.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-129+2689dupT | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201068920 | ||||||
chr2:201069007
|
C | T | 1 | a0001c0001t0005g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-129+2603G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069007 | ||||||
chr2:201069077
|
T | G | 1 | a0001c0001t0027g0033 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-129+2533A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069077 | ||||||
chr2:201069193
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+2417T>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069193 | ||||||
chr2:201069500
|
T | C | 11 | a0001c0001t0005g0019a0001c0001t0005g0147a0001c0001t0005g0148others(8): Show | 11 | HG02615.hp2 HG02886.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-129+2110A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069500 | ||||||
chr2:201069542
|
AAACAC | A | 2 | a0001c0001t0001g0034a0001c0001t0002g0035 | 2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-129+2063_-129+206 others(9): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069542 | ||||||
chr2:201069543
|
AAC | A | 19 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0022others(16): Show | 19 | HG01175.hp2 HG01192.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-129+2065_-129+206 others(6): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACAC | A | 18 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(15): Show | 18 | HG01496.hp1 HG01496.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.-129+2063_-129+206 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACAC | A | 23 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.-129+2061_-129+206 others(10): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(1): Show |
A | 19 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0076others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(16): Show |
intron_variant | MODIFIER | c.-129+2059_-129+206 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(3): Show |
A | 26 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0097others(23): Show | 27 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.-129+2057_-129+206 others(14): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(5): Show |
A | 28 | a0001c0001t0003g0120a0001c0001t0003g0127a0001c0001t0003g0128others(25): Show | 29 | HG00280.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.-129+2055_-129+206 others(16): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(7): Show |
A | 8 | a0001c0001t0003g0131a0001c0001t0003g0133a0001c0001t0003g0134others(5): Show | 8 | HG02630.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+2053_-129+206 others(18): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0136a0001c0001t0023g0137 | 2 | HG02055.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-129+2051_-129+206 others(20): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(13): Show |
A | 1 | a0001c0001t0006g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-129+2047_-129+206 others(24): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(15): Show |
A | 5 | a0001c0001t0008g0142a0001c0001t0014g0139a0001c0001t0014g0140others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-129+2045_-129+206 others(26): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(19): Show |
A | 5 | a0001c0001t0013g0003a0001c0001t0013g0005a0001c0001t0013g0145others(2): Show | 5 | HG01261.hp1 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-129+2041_-129+206 others(30): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069543
|
AACACACA others(25): Show |
A | 1 | a0001c0001t0043g0146 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-129+2035_-129+206 others(36): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069543 | ||||||
chr2:201069579
|
C | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+2031G>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | ||||||
chr2:201069579
|
C | CACAA | 8 | a0001c0001t0005g0152a0001c0001t0005g0153a0001c0001t0005g0154others(5): Show | 8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-129+2030_-129+203 others(8): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | ||||||
chr2:201069579
|
C | CACACACA others(1): Show |
2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-129+2030_-129+203 others(12): Show |
HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069579 | ||||||
chr2:201069614
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00558.hp1 HG01192.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-129+1996G>A | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201069614 | ||||||
chr2:201070095
|
A | G | 1 | a0001c0001t0032g0004 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-129+1515T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070095 | ||||||
chr2:201070307
|
A | G | 2 | a0001c0001t0013g0005a0001c0001t0032g0004 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-129+1303T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070307 | ||||||
chr2:201070451
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-129+1159C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070451 | ||||||
chr2:201070649
|
T | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+961A>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070649 | ||||||
chr2:201070677
|
T | C | 13 | a0001c0001t0002g0158a0001c0001t0003g0161a0001c0001t0003g0162others(10): Show | 13 | HG02280.hp2 HG02559.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-129+933A>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070677 | ||||||
chr2:201070781
|
T | G | 1 | a0001c0001t0011g0170 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-129+829A>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201070781 | ||||||
chr2:201071002
|
A | G | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+608T>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071002 | ||||||
chr2:201071077
|
G | C | 1 | a0001c0001t0008g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-129+533C>G | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071077 | ||||||
chr2:201071138
|
G | A | 1 | a0001c0001t0034g0172 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-129+472C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071138 | ||||||
chr2:201071279
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-129+331C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071279 | ||||||
chr2:201071303
|
G | A | 1 | a0001c0001t0021g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-129+307C>T | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071303 | ||||||
chr2:201071378
|
C | G | 1 | a0001c0001t0013g0003 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-129+232G>C | HYCC2 | ENSG00000155744.10 | transcript | ENST00000681958.1 | protein_coding | 1/12 | chr2 | 201071378 |