Item | Value |
---|---|
geneid | 64426 |
ensemblid | ENSG00000111707.12 |
hgncid | 29545 |
symbol | SUDS3 |
name | SDS3 homolog, SIN3A corepressor complex component |
refseq_nuc | NM_022491.3 |
refseq_prot | NP_071936.2 |
ensembl_nuc | ENST00000543473.2 |
ensembl_prot | ENSP00000443988.1 |
mane_status | MANE Select |
chr | chr12 |
start | 118376555 |
end | 118418033 |
strand | + |
ver | v1.2 |
region | chr12:118376555-118418033 |
region5000 | chr12:118371555-118423033 |
regionname0 | SUDS3_chr12_118376555_118418033 |
regionname5000 | SUDS3_chr12_118371555_118423033 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 984 | 408 | 92 | 66 | 194 | 18 | 36 | SUDS3_chr12_118371555_118423033 | SUDS3 | ATGAG others(979): Show |
chr12 | 118371555 | 118423033 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4724 | 108 | 14 | 11 | 68 | 5 | 10 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0002 | 1/1 | 4724 | 103 | 17 | 19 | 53 | 3 | 9 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0003 | 0/0 | 4724 | 40 | 0 | 0 | 40 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0004 | 0/0 | 4724 | 24 | 1 | 7 | 14 | 0 | 2 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0005 | 0/0 | 4722 | 13 | 0 | 4 | 2 | 3 | 4 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4717): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0006 | 0/0 | 4723 | 12 | 0 | 4 | 0 | 5 | 3 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0007 | 0/0 | 4723 | 10 | 6 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0008 | 0/0 | 4726 | 9 | 9 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4721): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0009 | 0/0 | 4723 | 9 | 9 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0010 | 0/0 | 4723 | 8 | 1 | 5 | 0 | 1 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0011 | 0/0 | 4722 | 7 | 7 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4717): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0012 | 0/0 | 4724 | 6 | 6 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0013 | 0/0 | 4724 | 6 | 6 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0014 | 0/0 | 4724 | 5 | 0 | 5 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0015 | 0/0 | 4724 | 4 | 0 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0016 | 0/0 | 4723 | 3 | 3 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0017 | 0/0 | 4725 | 3 | 0 | 1 | 1 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0018 | 0/0 | 4724 | 3 | 0 | 2 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0019 | 0/0 | 4722 | 2 | 0 | 2 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4717): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0020 | 0/0 | 4724 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0021 | 0/0 | 4724 | 2 | 0 | 2 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0022 | 0/0 | 4725 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0023 | 0/0 | 4724 | 2 | 0 | 0 | 0 | 0 | 2 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0024 | 0/0 | 4724 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0025 | 0/0 | 4725 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0026 | 0/0 | 4724 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0027 | 0/0 | 4724 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0028 | 0/0 | 4724 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0029 | 0/0 | 4724 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0030 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0031 | 0/0 | 4724 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0032 | 0/0 | 4724 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0033 | 0/0 | 4724 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0034 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0035 | 0/0 | 4723 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0036 | 0/0 | 4724 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0037 | 0/0 | 4724 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0038 | 0/0 | 4725 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0039 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0040 | 0/0 | 4725 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0041 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0042 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4718): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0043 | 0/0 | 4724 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4719): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0044 | 0/0 | 4725 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0045 | 0/0 | 4725 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
a0001c0001t0046 | 0/0 | 4725 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | GGAGA others(4720): Show |
chr12 | 118371555 | 118423033 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0001 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0010 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0008g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0008g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0008g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0008g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0010g0002 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0010g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0013g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0013g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0014g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0014g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0014g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0014g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0014g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0015g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0015g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0016g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0017g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0017g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0017g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0018g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0018g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0018g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0019g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0020g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0021g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0021g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0022g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0023g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0023g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0024g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0024g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0025g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0025g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0026g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0027g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0028g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0029g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0030g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0031g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0032g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0033g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0034g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0035g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0036g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0037g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0038g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0039g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0040g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0041g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0042g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0043g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0044g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0045g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
a0001c0001t0046g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0322 | EUR | GBR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | GBR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00140 | hp1 | a0001 | c0001 | t0010 | g0002 | EUR | GBR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0046 | EUR | FIN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0326 | EUR | FIN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00558 | hp2 | a0001 | c0001 | t0020 | g0003 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0300 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00642 | hp1 | a0001 | c0001 | t0019 | g0047 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | CHS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00735 | hp2 | a0001 | c0001 | t0017 | g0112 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0323 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01070 | hp1 | a0001 | c0001 | t0033 | g0030 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0002 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01074 | hp2 | a0001 | c0001 | t0029 | g0025 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0293 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01167 | hp1 | a0001 | c0001 | t0035 | g0189 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0294 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01175 | hp1 | a0001 | c0001 | t0018 | g0198 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0197 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01255 | hp2 | a0001 | c0001 | t0019 | g0047 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01257 | hp2 | a0001 | c0001 | t0014 | g0193 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0040 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01258 | hp2 | a0001 | c0001 | t0010 | g0002 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01358 | hp1 | a0001 | c0001 | t0021 | g0158 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01496 | hp1 | a0001 | c0001 | t0034 | g0192 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0299 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0296 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01516 | hp2 | a0001 | c0001 | t0017 | g0096 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0297 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0045 | EUR | IBS | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0085 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0028 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01978 | hp2 | a0001 | c0001 | t0014 | g0168 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0321 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02004 | hp1 | a0001 | c0001 | t0021 | g0130 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0086 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02056 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02135 | hp2 | a0001 | c0001 | t0007 | g0276 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0313 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02148 | hp1 | a0001 | c0001 | t0018 | g0190 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02155 | hp2 | a0001 | c0001 | t0038 | g0201 | EAS | CDX | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CDX | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02257 | hp1 | a0001 | c0001 | t0045 | g0316 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0002 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02293 | hp2 | a0001 | c0001 | t0014 | g0195 | AMR | PEL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02451 | hp1 | a0001 | c0001 | t0016 | g0058 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0027 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0310 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02602 | hp1 | a0001 | c0001 | t0018 | g0191 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0059 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0020 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0062 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0311 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02683 | hp2 | a0001 | c0001 | t0023 | g0262 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0327 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02723 | hp1 | a0001 | c0001 | t0039 | g0067 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0054 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02886 | hp2 | a0001 | c0001 | t0022 | g0222 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0165 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02922 | hp2 | a0001 | c0001 | t0011 | g0064 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0268 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0053 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0283 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03017 | hp2 | a0001 | c0001 | t0036 | g0260 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03041 | hp1 | a0001 | c0001 | t0009 | g0087 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03041 | hp2 | a0001 | c0001 | t0030 | g0304 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03098 | hp1 | a0001 | c0001 | t0042 | g0103 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0282 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0164 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03139 | hp1 | a0001 | c0001 | t0025 | g0269 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0052 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0084 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0065 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0320 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03491 | hp2 | a0001 | c0001 | t0043 | g0175 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03540 | hp1 | a0001 | c0001 | t0046 | g0319 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03540 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | GWD | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03579 | hp1 | a0001 | c0001 | t0025 | g0318 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03579 | hp2 | a0001 | c0001 | t0012 | g0167 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | STU | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0328 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0200 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0324 | SAS | PJL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0298 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03831 | hp2 | a0001 | c0001 | t0026 | g0077 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03834 | hp1 | a0001 | c0001 | t0023 | g0171 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03927 | hp1 | a0001 | c0001 | t0028 | g0110 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0301 | SAS | STU | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0073 | SAS | STU | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18522 | hp1 | a0001 | c0001 | t0044 | g0317 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18522 | hp2 | a0001 | c0001 | t0024 | g0105 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18612 | hp1 | a0001 | c0001 | t0020 | g0003 | EAS | CHB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18906 | hp1 | a0001 | c0001 | t0022 | g0212 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18906 | hp2 | a0001 | c0001 | t0012 | g0309 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18949 | hp1 | a0001 | c0001 | t0032 | g0254 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18977 | hp1 | a0001 | c0001 | t0027 | g0012 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0278 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18992 | hp1 | a0001 | c0001 | t0015 | g0021 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18995 | hp2 | a0001 | c0001 | t0017 | g0155 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18998 | hp1 | a0001 | c0001 | t0040 | g0292 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18999 | hp1 | a0001 | c0001 | t0015 | g0021 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19030 | hp1 | a0001 | c0001 | t0024 | g0106 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19043 | hp2 | a0001 | c0001 | t0013 | g0163 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19062 | hp2 | a0001 | c0001 | t0031 | g0051 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19067 | hp1 | a0001 | c0001 | t0037 | g0241 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19079 | hp2 | a0001 | c0001 | t0015 | g0100 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19080 | hp2 | a0001 | c0001 | t0015 | g0098 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0325 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19090 | hp2 | a0001 | c0001 | t0007 | g0291 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0314 | AFR | ASW | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ASW | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | TSI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0045 | EUR | TSI | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0302 | SAS | GIH | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01123 | hp1 | a0001 | c0001 | t0014 | g0194 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG02559 | hp2 | a0001 | c0001 | t0041 | g0063 | AFR | ACB | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0315 | AFR | MSL | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | USA | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | USA | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | USA | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | USA | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0166 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0187 | REF | REF | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0010 | REF | REF | SUDS3_chr12_118371555_118423033 | SUDS3 | chr12 | 118371555 | 118423033 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:118414607 | A | G | 4 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(1): Show |
5 | HG02257.hp1 HG03139.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*174A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 174 | chr12 | 118414607 | ||||||
chr12:118414638 | C | T | 1 | a0001c0001t0043 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 205 | chr12 | 118414638 | ||||||
chr12:118414682 | G | A | 1 | a0001c0001t0026 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 249 | chr12 | 118414682 | ||||||
chr12:118414812 | C | T | 1 | a0001c0001t0042 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 379 | chr12 | 118414812 | ||||||
chr12:118414906 | G | C | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0019 others(4): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*473G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 473 | chr12 | 118414906 | ||||||
chr12:118415016 | C | T | 2 | a0001c0001t0008 a0001c0001t0046 |
10 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*583C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 583 | chr12 | 118415016 | ||||||
chr12:118415034 | A | G | 4 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(1): Show |
5 | HG02257.hp1 HG03139.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*601A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 601 | chr12 | 118415034 | ||||||
chr12:118415067 | A | G | 1 | a0001c0001t0041 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 634 | chr12 | 118415067 | ||||||
chr12:118415137 | A | T | 2 | a0001c0001t0044 a0001c0001t0045 |
2 | HG02257.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*704A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 704 | chr12 | 118415137 | ||||||
chr12:118415144 | G | A | 1 | a0001c0001t0027 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*711G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 711 | chr12 | 118415144 | ||||||
chr12:118415434 | G | A | 1 | a0001c0001t0028 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1001G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1001 | chr12 | 118415434 | ||||||
chr12:118415465 | G | C | 1 | a0001c0001t0019 | 2 | HG00642.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1032G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1032 | chr12 | 118415465 | ||||||
chr12:118415632 | C | A | 1 | a0001c0001t0029 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1199C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1199 | chr12 | 118415632 | ||||||
chr12:118415662 | C | T | 2 | a0001c0001t0018 a0001c0001t0046 |
4 | HG01175.hp1 HG02148.hp1 HG02602.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1229 | chr12 | 118415662 | ||||||
chr12:118415664 | T | C | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1231T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1231 | chr12 | 118415664 | ||||||
chr12:118415665 | C | G | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1232C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1232 | chr12 | 118415665 | ||||||
chr12:118415704 | T | C | 1 | a0001c0001t0044 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1271T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1271 | chr12 | 118415704 | ||||||
chr12:118415708 | T | C | 1 | a0001c0001t0009 | 9 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1275 | chr12 | 118415708 | ||||||
chr12:118415723 | C | T | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1290 | chr12 | 118415723 | ||||||
chr12:118415724 | T | C | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1291T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1291 | chr12 | 118415724 | ||||||
chr12:118415783 | TGGG | T | 2 | a0001c0001t0005 a0001c0001t0019 |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1354_*1356delGGG | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1354 | INFO_REALIGN_3_PRIME | chr12 | 118415783 | |||||
chr12:118415897 | T | A | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1464T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1464 | chr12 | 118415897 | ||||||
chr12:118415916 | G | A | 1 | a0001c0001t0020 | 2 | HG00558.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1483G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1483 | chr12 | 118415916 | ||||||
chr12:118415926 | CT | C | 9 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(6): Show |
82 | HG00140.hp1 HG00558.hp2 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1509delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1509 | INFO_REALIGN_3_PRIME | chr12 | 118415926 | |||||
chr12:118416083 | A | C | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1650A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1650 | chr12 | 118416083 | ||||||
chr12:118416265 | A | G | 1 | a0001c0001t0024 | 2 | NA18522.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1832A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1832 | chr12 | 118416265 | ||||||
chr12:118416391 | T | TG | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0019 others(4): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1959dupG | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 1960 | INFO_REALIGN_3_PRIME | chr12 | 118416391 | |||||
chr12:118416513 | C | T | 1 | a0001c0001t0013 | 6 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2080C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2080 | chr12 | 118416513 | ||||||
chr12:118416602 | A | G | 2 | a0001c0001t0005 a0001c0001t0019 |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2169A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2169 | chr12 | 118416602 | ||||||
chr12:118416695 | G | A | 1 | a0001c0001t0021 | 2 | HG01358.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2262G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2262 | chr12 | 118416695 | ||||||
chr12:118416771 | G | A | 1 | a0001c0001t0032 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2338 | chr12 | 118416771 | ||||||
chr12:118416793 | T | G | 1 | a0001c0001t0045 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2360 | chr12 | 118416793 | ||||||
chr12:118416799 | C | A | 1 | a0001c0001t0033 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2366C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2366 | chr12 | 118416799 | ||||||
chr12:118416813 | G | T | 1 | a0001c0001t0006 | 12 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2380G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2380 | chr12 | 118416813 | ||||||
chr12:118416848 | A | G | 4 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(1): Show |
5 | HG02257.hp1 HG03139.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2415A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2415 | chr12 | 118416848 | ||||||
chr12:118416879 | T | A | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2446T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2446 | chr12 | 118416879 | ||||||
chr12:118416958 | G | A | 1 | a0001c0001t0008 | 9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2525G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2525 | chr12 | 118416958 | ||||||
chr12:118416999 | A | G | 10 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0017 others(7): Show |
124 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2566A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2566 | chr12 | 118416999 | ||||||
chr12:118417008 | G | T | 4 | a0001c0001t0025 a0001c0001t0044 a0001c0001t0045 others(1): Show |
5 | HG02257.hp1 HG03139.hp1 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2575G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2575 | chr12 | 118417008 | ||||||
chr12:118417012 | C | G | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2579C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2579 | chr12 | 118417012 | ||||||
chr12:118417013 | G | C | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2580G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2580 | chr12 | 118417013 | ||||||
chr12:118417050 | G | T | 1 | a0001c0001t0015 | 4 | NA18992.hp1 NA18999.hp1 NA19079.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2617G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2617 | chr12 | 118417050 | ||||||
chr12:118417267 | C | T | 18 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(15): Show |
113 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2834C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 2834 | chr12 | 118417267 | ||||||
chr12:118417479 | T | A | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0019 others(4): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3046T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3046 | chr12 | 118417479 | ||||||
chr12:118417505 | A | G | 1 | a0001c0001t0023 | 2 | HG02683.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3072A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3072 | chr12 | 118417505 | ||||||
chr12:118417600 | A | G | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(30): Show |
278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*3167A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3167 | chr12 | 118417600 | ||||||
chr12:118417627 | G | A | 3 | a0001c0001t0014 a0001c0001t0018 a0001c0001t0034 |
9 | HG01123.hp1 HG01175.hp1 HG01255.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3194G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3194 | chr12 | 118417627 | ||||||
chr12:118417674 | T | C | 1 | a0001c0001t0016 | 3 | HG02451.hp1 HG02615.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3241T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3241 | chr12 | 118417674 | ||||||
chr12:118417677 | G | GT | 9 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0017 others(6): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*3259dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3260 | INFO_REALIGN_3_PRIME | chr12 | 118417677 | |||||
chr12:118417677 | GT | G | 7 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0016 others(4): Show |
23 | HG01167.hp1 HG01496.hp1 HG01884.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3259delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3259 | INFO_REALIGN_3_PRIME | chr12 | 118417677 | |||||
chr12:118417678 | T | G | 2 | a0001c0001t0005 a0001c0001t0019 |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3245T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3245 | chr12 | 118417678 | ||||||
chr12:118417761 | G | A | 2 | a0001c0001t0005 a0001c0001t0019 |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3328G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3328 | chr12 | 118417761 | ||||||
chr12:118417772 | T | G | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3339T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3339 | chr12 | 118417772 | ||||||
chr12:118417799 | A | G | 1 | a0001c0001t0037 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3366A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3366 | chr12 | 118417799 | ||||||
chr12:118417908 | A | G | 1 | a0001c0001t0036 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3475A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3475 | chr12 | 118417908 | ||||||
chr12:118418008 | T | C | 9 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0012 others(6): Show |
41 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3575T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3575 | chr12 | 118418008 | ||||||
chr12:118418018 | A | T | 1 | a0001c0001t0030 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3585A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 12/12 | 3585 | chr12 | 118418018 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:118376953 | G | C | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.142+120G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118376953 | |||||||
chr12:118376953 | G | T | 1 | a0001c0001t0001g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.142+120G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118376953 | |||||||
chr12:118377033 | C | T | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.142+200C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377033 | |||||||
chr12:118377091 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.142+258C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377091 | |||||||
chr12:118377136 | A | G | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142+303A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377136 | |||||||
chr12:118377227 | C | T | 6 | a0001c0001t0001g0303 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02451.hp2 HG03041.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+394C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377227 | |||||||
chr12:118377271 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.142+438G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377271 | |||||||
chr12:118377306 | C | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(46): Show |
64 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.142+473C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377306 | |||||||
chr12:118377467 | A | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.142+634A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377467 | |||||||
chr12:118377483 | G | A | 2 | a0001c0001t0008g0313 a0001c0001t0008g0314 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142+650G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377483 | |||||||
chr12:118377529 | C | G | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.142+696C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377529 | |||||||
chr12:118377565 | G | A | 3 | a0001c0001t0005g0320 a0001c0001t0005g0321 a0001c0001t0005g0322 |
3 | HG00099.hp1 HG01993.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.142+732G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377565 | |||||||
chr12:118377604 | C | G | 113 | a0001c0001t0001g0035 a0001c0001t0001g0176 a0001c0001t0001g0180 others(110): Show |
130 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.142+771C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377604 | |||||||
chr12:118377632 | T | A | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+799T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377632 | |||||||
chr12:118377661 | G | T | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+828G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377661 | |||||||
chr12:118377675 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0010g0040 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.142+842A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377675 | |||||||
chr12:118377691 | G | T | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+858G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377691 | |||||||
chr12:118377697 | G | A | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+864G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377697 | |||||||
chr12:118377699 | A | G | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+866A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377699 | |||||||
chr12:118377764 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.142+931C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377764 | |||||||
chr12:118377894 | G | A | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+1061G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377894 | |||||||
chr12:118377895 | A | G | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+1062A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377895 | |||||||
chr12:118377896 | A | G | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+1063A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377896 | |||||||
chr12:118377897 | G | C | 1 | a0001c0001t0031g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.142+1064G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377897 | |||||||
chr12:118377952 | C | T | 7 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+1119C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377952 | |||||||
chr12:118377983 | T | C | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.142+1150T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377983 | |||||||
chr12:118377992 | G | A | 1 | a0001c0001t0014g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.142+1159G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118377992 | |||||||
chr12:118378122 | TC | T | 2 | a0001c0001t0007g0041 a0001c0001t0007g0265 |
3 | HG02622.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.142+1291delC | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 118378122 | ||||||
chr12:118378176 | A | G | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142+1343A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378176 | |||||||
chr12:118378271 | T | C | 2 | a0001c0001t0008g0014 a0001c0001t0008g0315 |
4 | HG01884.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+1438T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378271 | |||||||
chr12:118378482 | C | CT | 37 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0003g0003 others(34): Show |
51 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.143-1663dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 118378482 | ||||||
chr12:118378482 | C | CTT | 11 | a0001c0001t0006g0045 a0001c0001t0006g0293 a0001c0001t0006g0294 others(8): Show |
12 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.143-1664_143-1663d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 118378482 | ||||||
chr12:118378482 | CT | C | 16 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
16 | HG01069.hp1 HG01070.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.143-1663delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr12 | 118378482 | ||||||
chr12:118378678 | A | G | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.143-1484A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378678 | |||||||
chr12:118378684 | T | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.143-1478T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378684 | |||||||
chr12:118378796 | C | T | 1 | a0001c0001t0023g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.143-1366C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378796 | |||||||
chr12:118378864 | G | A | 2 | a0001c0001t0016g0058 a0001c0001t0016g0059 |
2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.143-1298G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378864 | |||||||
chr12:118378910 | G | A | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.143-1252G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118378910 | |||||||
chr12:118379142 | A | G | 1 | a0001c0001t0002g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.143-1020A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379142 | |||||||
chr12:118379234 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.143-928C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379234 | |||||||
chr12:118379257 | C | T | 2 | a0001c0001t0025g0318 a0001c0001t0046g0319 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.143-905C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379257 | |||||||
chr12:118379578 | C | T | 1 | a0001c0001t0036g0260 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.143-584C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379578 | |||||||
chr12:118379949 | T | A | 1 | a0001c0001t0002g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.143-213T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379949 | |||||||
chr12:118379956 | T | G | 3 | a0001c0001t0013g0027 a0001c0001t0013g0028 a0001c0001t0013g0163 |
5 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-206T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118379956 | |||||||
chr12:118380025 | C | G | 46 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(43): Show |
60 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.143-137C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118380025 | |||||||
chr12:118380044 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0043g0175 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.143-118G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118380044 | |||||||
chr12:118380072 | G | A | 114 | a0001c0001t0001g0068 a0001c0001t0003g0003 a0001c0001t0003g0008 others(111): Show |
146 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.143-90G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118380072 | |||||||
chr12:118380107 | C | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | NA18962.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.143-55C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 1/11 | chr12 | 118380107 | |||||||
chr12:118380381 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.212+150T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380381 | |||||||
chr12:118380502 | A | C | 1 | a0001c0001t0004g0081 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.212+271A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380502 | |||||||
chr12:118380518 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0169 |
3 | HG01975.hp1 HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.212+287G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380518 | |||||||
chr12:118380553 | C | A | 49 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(46): Show |
64 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.212+322C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380553 | |||||||
chr12:118380554 | A | T | 49 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(46): Show |
64 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.212+323A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380554 | |||||||
chr12:118380615 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.212+384G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380615 | |||||||
chr12:118380654 | A | G | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.212+423A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380654 | |||||||
chr12:118380660 | C | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.212+429C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380660 | |||||||
chr12:118380797 | C | T | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.212+566C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118380797 | |||||||
chr12:118381011 | T | C | 2 | a0001c0001t0012g0309 a0001c0001t0012g0310 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.212+780T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381011 | |||||||
chr12:118381120 | G | C | 3 | a0001c0001t0005g0326 a0001c0001t0005g0327 a0001c0001t0005g0328 |
3 | HG00323.hp1 HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.212+889G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381120 | |||||||
chr12:118381211 | AT | A | 14 | a0001c0001t0001g0180 a0001c0001t0005g0046 a0001c0001t0005g0048 others(11): Show |
16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.212+991delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118381211 | ||||||
chr12:118381239 | C | T | 3 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 |
3 | HG02896.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.212+1008C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381239 | |||||||
chr12:118381359 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.212+1128C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381359 | |||||||
chr12:118381507 | C | T | 1 | a0001c0001t0040g0292 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.212+1276C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381507 | |||||||
chr12:118381688 | C | G | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(41): Show |
56 | HG00642.hp2 HG00673.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.212+1457C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381688 | |||||||
chr12:118381757 | TCAGA | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.212+1531_212+1534d others(6): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118381757 | ||||||
chr12:118381902 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.212+1671G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118381902 | |||||||
chr12:118382001 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.212+1770G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382001 | |||||||
chr12:118382044 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0115 others(13): Show |
17 | HG00140.hp2 HG02040.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.212+1826dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382044 | ||||||
chr12:118382254 | G | A | 14 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 others(11): Show |
15 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.213-1758G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382254 | |||||||
chr12:118382344 | G | GGCCACTT others(15): Show |
1 | a0001c0001t0036g0260 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.213-1645_213-1624d others(24): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382344 | ||||||
chr12:118382344 | GGCCACTT others(15): Show |
G | 119 | a0001c0001t0001g0068 a0001c0001t0002g0039 a0001c0001t0002g0257 others(116): Show |
152 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.213-1645_213-1624d others(24): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382344 | ||||||
chr12:118382430 | C | T | 1 | a0001c0001t0011g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213-1582C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382430 | |||||||
chr12:118382603 | G | A | 16 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(13): Show |
18 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.213-1409G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382603 | |||||||
chr12:118382618 | C | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.213-1394C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382618 | |||||||
chr12:118382666 | CT | C | 14 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0115 others(11): Show |
15 | HG00323.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.213-1329delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382666 | ||||||
chr12:118382666 | CTTT | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.213-1331_213-1329d others(5): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382666 | ||||||
chr12:118382669 | T | C | 2 | a0001c0001t0044g0317 a0001c0001t0045g0316 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.213-1343T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382669 | |||||||
chr12:118382737 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 |
3 | HG02040.hp2 HG02155.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.213-1275G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382737 | |||||||
chr12:118382780 | G | T | 1 | a0001c0001t0044g0317 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.213-1232G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382780 | |||||||
chr12:118382834 | A | AT | 237 | a0001c0001t0001g0035 a0001c0001t0001g0068 a0001c0001t0001g0111 others(234): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.213-1166dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118382834 | ||||||
chr12:118382901 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.213-1111C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382901 | |||||||
chr12:118382914 | C | G | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.213-1098C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382914 | |||||||
chr12:118382922 | C | T | 1 | a0001c0001t0045g0316 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213-1090C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118382922 | |||||||
chr12:118383078 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.213-934G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383078 | |||||||
chr12:118383151 | C | T | 1 | a0001c0001t0006g0302 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.213-861C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383151 | |||||||
chr12:118383165 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(1): Show |
4 | NA18939.hp2 NA18966.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.213-847T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383165 | |||||||
chr12:118383434 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.213-578T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383434 | |||||||
chr12:118383486 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18944.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.213-526C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383486 | |||||||
chr12:118383507 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.213-505C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383507 | |||||||
chr12:118383633 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.213-379C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383633 | |||||||
chr12:118383635 | A | G | 1 | a0001c0001t0032g0254 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.213-377A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383635 | |||||||
chr12:118383650 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.213-362T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383650 | |||||||
chr12:118383942 | G | T | 1 | a0001c0001t0009g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.213-70G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | chr12 | 118383942 | |||||||
chr12:118383995 | C | CT | 14 | a0001c0001t0002g0253 a0001c0001t0005g0046 a0001c0001t0005g0048 others(11): Show |
16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.213-5dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118383995 | ||||||
chr12:118383995 | CT | C | 69 | a0001c0001t0001g0068 a0001c0001t0003g0003 a0001c0001t0003g0008 others(66): Show |
92 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(89): Show |
splice_region_variant&intron_variant | LOW | c.213-5delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr12 | 118383995 | ||||||
chr12:118384171 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.268+104G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384171 | |||||||
chr12:118384251 | T | C | 1 | a0001c0001t0041g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.268+184T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384251 | |||||||
chr12:118384268 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.268+201G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384268 | |||||||
chr12:118384271 | T | C | 2 | a0001c0001t0002g0188 a0001c0001t0025g0269 |
2 | HG03139.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.268+204T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384271 | |||||||
chr12:118384316 | A | G | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+249A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384316 | |||||||
chr12:118384570 | C | T | 1 | a0001c0001t0021g0158 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.268+503C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384570 | |||||||
chr12:118384669 | G | A | 111 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(108): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.268+602G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384669 | |||||||
chr12:118384918 | A | C | 1 | a0001c0001t0002g0252 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.268+851A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118384918 | |||||||
chr12:118385113 | T | C | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-1001T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385113 | |||||||
chr12:118385125 | T | G | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-989T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385125 | |||||||
chr12:118385127 | G | A | 1 | a0001c0001t0035g0189 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.269-987G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385127 | |||||||
chr12:118385269 | C | T | 27 | a0001c0001t0002g0038 a0001c0001t0002g0173 a0001c0001t0002g0177 others(24): Show |
28 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.269-845C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385269 | |||||||
chr12:118385367 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.269-747T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385367 | |||||||
chr12:118385429 | T | C | 13 | a0001c0001t0002g0185 a0001c0001t0002g0196 a0001c0001t0002g0199 others(10): Show |
13 | HG01123.hp1 HG01175.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.269-685T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385429 | |||||||
chr12:118385476 | G | T | 15 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0013 others(12): Show |
23 | HG00558.hp2 HG00673.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.269-638G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385476 | |||||||
chr12:118385842 | C | G | 1 | a0001c0001t0008g0314 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.269-272C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 3/11 | chr12 | 118385842 | |||||||
chr12:118386478 | T | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+293T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118386478 | |||||||
chr12:118386522 | T | C | 1 | a0001c0001t0003g0044 | 2 | HG02040.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.340+337T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118386522 | |||||||
chr12:118386527 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.340+342G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118386527 | |||||||
chr12:118386791 | A | G | 1 | a0001c0001t0009g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.340+606A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118386791 | |||||||
chr12:118386926 | C | T | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.340+741C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118386926 | |||||||
chr12:118387024 | C | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+839C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387024 | |||||||
chr12:118387213 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0119 |
3 | NA18947.hp2 NA18950.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.340+1028C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387213 | |||||||
chr12:118387213 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.340+1028C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387213 | |||||||
chr12:118387400 | T | C | 1 | a0001c0001t0002g0255 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.340+1215T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387400 | |||||||
chr12:118387698 | C | T | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+1513C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387698 | |||||||
chr12:118387800 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.340+1615C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387800 | |||||||
chr12:118387807 | T | C | 5 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0006g0295 others(2): Show |
5 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1622T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118387807 | |||||||
chr12:118388162 | C | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.341-1765C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388162 | |||||||
chr12:118388204 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.341-1723A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388204 | |||||||
chr12:118388413 | T | C | 1 | a0001c0001t0012g0165 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-1514T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388413 | |||||||
chr12:118388425 | C | T | 1 | a0001c0001t0007g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.341-1502C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388425 | |||||||
chr12:118388454 | T | G | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.341-1473T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388454 | |||||||
chr12:118388548 | C | T | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.341-1379C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388548 | |||||||
chr12:118388816 | C | T | 2 | a0001c0001t0007g0268 a0001c0001t0007g0282 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.341-1111C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388816 | |||||||
chr12:118388860 | A | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1067A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118388860 | |||||||
chr12:118389230 | G | A | 6 | a0001c0001t0003g0003 a0001c0001t0003g0044 a0001c0001t0003g0114 others(3): Show |
11 | HG00558.hp2 HG02040.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.341-697G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118389230 | |||||||
chr12:118389462 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.341-465C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118389462 | |||||||
chr12:118389512 | A | AT | 14 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0303 others(11): Show |
14 | HG01167.hp1 HG01175.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-398dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr12 | 118389512 | ||||||
chr12:118389661 | G | A | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.341-266G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118389661 | |||||||
chr12:118389721 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.341-206G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 4/11 | chr12 | 118389721 | |||||||
chr12:118389976 | G | A | 51 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(48): Show |
67 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.360+30G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118389976 | |||||||
chr12:118390127 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0017g0155 a0001c0001t0025g0269 |
4 | HG03139.hp1 NA18960.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+181C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390127 | |||||||
chr12:118390166 | T | C | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.360+220T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390166 | |||||||
chr12:118390266 | A | G | 1 | a0001c0001t0039g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.360+320A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390266 | |||||||
chr12:118390302 | G | A | 1 | a0001c0001t0010g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.360+356G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390302 | |||||||
chr12:118390426 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.360+480A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390426 | |||||||
chr12:118390560 | G | A | 2 | a0001c0001t0009g0060 a0001c0001t0009g0061 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.361-566G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390560 | |||||||
chr12:118390651 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.361-475G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390651 | |||||||
chr12:118390682 | G | A | 9 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(6): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.361-444G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390682 | |||||||
chr12:118390737 | T | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.361-389T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390737 | |||||||
chr12:118390756 | T | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-370T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390756 | |||||||
chr12:118390950 | G | A | 114 | a0001c0001t0001g0035 a0001c0001t0001g0176 a0001c0001t0001g0180 others(111): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.361-176G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390950 | |||||||
chr12:118390971 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.361-155C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390971 | |||||||
chr12:118390972 | G | T | 2 | a0001c0001t0044g0317 a0001c0001t0045g0316 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.361-154G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390972 | |||||||
chr12:118390975 | G | A | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.361-151G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390975 | |||||||
chr12:118390996 | A | G | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.361-130A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118390996 | |||||||
chr12:118391121 | C | T | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.361-5C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 5/11 | chr12 | 118391121 | |||||||
chr12:118391324 | G | C | 2 | a0001c0001t0007g0041 a0001c0001t0007g0265 |
3 | HG02622.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.517+42G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118391324 | |||||||
chr12:118391502 | C | G | 4 | a0001c0001t0006g0045 a0001c0001t0006g0299 a0001c0001t0006g0300 others(1): Show |
5 | HG00639.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+220C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118391502 | |||||||
chr12:118391829 | C | G | 1 | a0001c0001t0002g0037 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.517+547C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118391829 | |||||||
chr12:118391855 | G | T | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+573G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118391855 | |||||||
chr12:118392128 | G | A | 29 | a0001c0001t0002g0038 a0001c0001t0002g0173 a0001c0001t0002g0177 others(26): Show |
30 | HG00423.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.517+846G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392128 | |||||||
chr12:118392201 | G | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+919G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392201 | |||||||
chr12:118392211 | G | A | 7 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+929G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392211 | |||||||
chr12:118392293 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.517+1011T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392293 | |||||||
chr12:118392616 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.517+1334C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392616 | |||||||
chr12:118392684 | C | A | 1 | a0001c0001t0003g0114 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.517+1402C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392684 | |||||||
chr12:118392789 | A | T | 5 | a0001c0001t0016g0058 a0001c0001t0016g0059 a0001c0001t0016g0066 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+1507A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392789 | |||||||
chr12:118392816 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.517+1534C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392816 | |||||||
chr12:118392817 | G | A | 6 | a0001c0001t0006g0045 a0001c0001t0006g0298 a0001c0001t0006g0299 others(3): Show |
7 | HG00639.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1535G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392817 | |||||||
chr12:118392841 | T | G | 1 | a0001c0001t0005g0324 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.517+1559T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392841 | |||||||
chr12:118392851 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.517+1569A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118392851 | |||||||
chr12:118393035 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.517+1753G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393035 | |||||||
chr12:118393153 | A | G | 291 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(288): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.517+1871A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393153 | |||||||
chr12:118393155 | A | G | 1 | a0001c0001t0025g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517+1873A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393155 | |||||||
chr12:118393250 | A | G | 7 | a0001c0001t0001g0113 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
7 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+1968A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393250 | |||||||
chr12:118393280 | A | T | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.517+1998A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393280 | |||||||
chr12:118393282 | T | C | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.517+2000T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393282 | |||||||
chr12:118393399 | G | A | 1 | a0001c0001t0013g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.517+2117G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393399 | |||||||
chr12:118393566 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.517+2284C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393566 | |||||||
chr12:118393609 | C | T | 115 | a0001c0001t0001g0035 a0001c0001t0001g0176 a0001c0001t0001g0180 others(112): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.517+2327C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393609 | |||||||
chr12:118393628 | G | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+2346G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393628 | |||||||
chr12:118393647 | ATTTC | A | 5 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0006g0295 others(2): Show |
5 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+2377_517+2380d others(6): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118393647 | ||||||
chr12:118393659 | C | CT | 4 | a0001c0001t0002g0229 a0001c0001t0008g0015 a0001c0001t0008g0313 others(1): Show |
6 | HG02145.hp2 HG02257.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+2389dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118393659 | ||||||
chr12:118393691 | G | T | 1 | a0001c0001t0002g0261 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.517+2409G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393691 | |||||||
chr12:118393706 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.517+2424T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393706 | |||||||
chr12:118393707 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.517+2425G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393707 | |||||||
chr12:118393708 | T | G | 1 | a0001c0001t0002g0177 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.517+2426T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393708 | |||||||
chr12:118393859 | CAG | C | 2 | a0001c0001t0007g0041 a0001c0001t0007g0265 |
3 | HG02622.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.517+2578_517+2579d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393859 | |||||||
chr12:118393949 | G | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.517+2667G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393949 | |||||||
chr12:118393960 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0031g0051 |
3 | NA18961.hp2 NA18975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.517+2678C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393960 | |||||||
chr12:118393976 | T | G | 1 | a0001c0001t0007g0268 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.517+2694T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393976 | |||||||
chr12:118393998 | C | T | 2 | a0001c0001t0006g0296 a0001c0001t0006g0297 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.517+2716C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118393998 | |||||||
chr12:118394030 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+2748T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394030 | |||||||
chr12:118394109 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517+2827T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394109 | |||||||
chr12:118394189 | C | A | 2 | a0001c0001t0025g0318 a0001c0001t0046g0319 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.517+2907C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394189 | |||||||
chr12:118394478 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.517+3196C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394478 | |||||||
chr12:118394495 | T | C | 1 | a0001c0001t0007g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.517+3213T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394495 | |||||||
chr12:118394639 | G | A | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.517+3357G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394639 | |||||||
chr12:118394743 | A | G | 1 | a0001c0001t0002g0263 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517+3461A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394743 | |||||||
chr12:118394858 | G | T | 2 | a0001c0001t0002g0040 a0001c0001t0010g0040 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.517+3576G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394858 | |||||||
chr12:118394893 | G | A | 1 | a0001c0001t0004g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.517+3611G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118394893 | |||||||
chr12:118395030 | A | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+3748A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395030 | |||||||
chr12:118395036 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.517+3754G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395036 | |||||||
chr12:118395163 | A | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.517+3881A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395163 | |||||||
chr12:118395216 | G | GT | 42 | a0001c0001t0001g0023 a0001c0001t0001g0083 a0001c0001t0001g0102 others(39): Show |
44 | HG00323.hp2 HG01361.hp1 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.517+3961dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | G | GTT | 5 | a0001c0001t0001g0120 a0001c0001t0002g0170 a0001c0001t0013g0028 others(2): Show |
6 | HG01891.hp2 HG02615.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+3960_517+3961d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | G | T | 1 | a0001c0001t0009g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.517+3934G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395216 | |||||||
chr12:118395216 | GT | G | 132 | a0001c0001t0001g0035 a0001c0001t0001g0088 a0001c0001t0001g0113 others(129): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.517+3961delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | GTT | G | 6 | a0001c0001t0002g0184 a0001c0001t0002g0234 a0001c0001t0002g0235 others(3): Show |
6 | HG01515.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.517+3960_517+3961d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | GTTT | G | 18 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0321 others(15): Show |
24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.517+3959_517+3961d others(5): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0007g0041 a0001c0001t0007g0265 |
3 | HG02622.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.517+3950_517+3961d others(14): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395216 | GTTTTTTT others(8): Show |
G | 19 | a0001c0001t0001g0068 a0001c0001t0004g0006 a0001c0001t0004g0009 others(16): Show |
26 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.517+3947_517+3961d others(17): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118395216 | ||||||
chr12:118395232 | T | G | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.517+3950T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395232 | |||||||
chr12:118395326 | C | T | 1 | a0001c0001t0045g0316 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.517+4044C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395326 | |||||||
chr12:118395682 | C | A | 2 | a0001c0001t0039g0067 a0001c0001t0041g0063 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.517+4400C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395682 | |||||||
chr12:118395695 | T | G | 1 | a0001c0001t0025g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+4413T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395695 | |||||||
chr12:118395755 | G | A | 7 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+4473G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395755 | |||||||
chr12:118395927 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.517+4645A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395927 | |||||||
chr12:118395956 | A | G | 1 | a0001c0001t0039g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.517+4674A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395956 | |||||||
chr12:118395974 | C | G | 1 | a0001c0001t0005g0323 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.518-4685C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118395974 | |||||||
chr12:118396038 | G | A | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.518-4621G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396038 | |||||||
chr12:118396336 | A | G | 1 | a0001c0001t0003g0017 | 2 | NA18952.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.518-4323A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396336 | |||||||
chr12:118396493 | A | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0072 others(2): Show |
7 | HG00544.hp2 NA18941.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.518-4166A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396493 | |||||||
chr12:118396513 | C | G | 7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0008g0014 others(4): Show |
11 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.518-4146C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396513 | |||||||
chr12:118396776 | G | A | 2 | a0001c0001t0044g0317 a0001c0001t0045g0316 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.518-3883G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396776 | |||||||
chr12:118396897 | A | AG | 5 | a0001c0001t0001g0068 a0001c0001t0004g0069 a0001c0001t0004g0070 others(2): Show |
5 | NA18939.hp2 NA18966.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-3758dupG | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118396897 | ||||||
chr12:118396941 | G | T | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-3718G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396941 | |||||||
chr12:118396975 | G | T | 1 | a0001c0001t0040g0292 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.518-3684G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118396975 | |||||||
chr12:118397048 | C | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.518-3611C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397048 | |||||||
chr12:118397121 | C | T | 4 | a0001c0001t0013g0027 a0001c0001t0013g0028 a0001c0001t0013g0163 others(1): Show |
6 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-3538C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397121 | |||||||
chr12:118397168 | A | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.518-3491A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397168 | |||||||
chr12:118397200 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.518-3459G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397200 | |||||||
chr12:118397232 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-3427G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397232 | |||||||
chr12:118397444 | G | T | 3 | a0001c0001t0016g0058 a0001c0001t0016g0059 a0001c0001t0016g0066 |
3 | HG02451.hp1 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.518-3215G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397444 | |||||||
chr12:118397581 | C | T | 1 | a0001c0001t0012g0311 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.518-3078C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397581 | |||||||
chr12:118397592 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.518-3067C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397592 | |||||||
chr12:118397637 | G | C | 1 | a0001c0001t0003g0286 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.518-3022G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397637 | |||||||
chr12:118397679 | G | C | 2 | a0001c0001t0025g0318 a0001c0001t0046g0319 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.518-2980G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397679 | |||||||
chr12:118397724 | A | AT | 75 | a0001c0001t0001g0099 a0001c0001t0001g0129 a0001c0001t0003g0003 others(72): Show |
94 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.518-2922dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118397724 | ||||||
chr12:118397724 | A | ATT | 6 | a0001c0001t0003g0280 a0001c0001t0007g0291 a0001c0001t0025g0318 others(3): Show |
6 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-2923_518-2922d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118397724 | ||||||
chr12:118397724 | A | ATTT | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-2924_518-2922d others(5): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118397724 | ||||||
chr12:118397812 | G | A | 3 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0219 |
3 | HG00544.hp1 NA18943.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.518-2847G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397812 | |||||||
chr12:118397842 | C | T | 1 | a0001c0001t0009g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.518-2817C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397842 | |||||||
chr12:118397850 | G | A | 3 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 |
3 | HG01884.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.518-2809G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397850 | |||||||
chr12:118397857 | C | T | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-2802C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397857 | |||||||
chr12:118397882 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.518-2777C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118397882 | |||||||
chr12:118398185 | G | C | 1 | a0001c0001t0041g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-2474G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398185 | |||||||
chr12:118398236 | G | T | 12 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.518-2423G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398236 | |||||||
chr12:118398299 | A | G | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.518-2360A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398299 | |||||||
chr12:118398321 | C | A | 2 | a0001c0001t0008g0014 a0001c0001t0008g0315 |
4 | HG01884.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-2338C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398321 | |||||||
chr12:118398321 | C | T | 1 | a0001c0001t0004g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.518-2338C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398321 | |||||||
chr12:118398343 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-2316G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398343 | |||||||
chr12:118398358 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.518-2301C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398358 | |||||||
chr12:118398470 | G | GGT | 6 | a0001c0001t0003g0044 a0001c0001t0008g0014 a0001c0001t0008g0015 others(3): Show |
11 | HG01884.hp2 HG02040.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-2172_518-2171d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118398470 | ||||||
chr12:118398527 | G | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.518-2132G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398527 | |||||||
chr12:118398614 | C | CT | 117 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0135 others(114): Show |
131 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.518-2026dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118398614 | ||||||
chr12:118398614 | C | CTT | 14 | a0001c0001t0001g0088 a0001c0001t0001g0113 a0001c0001t0001g0303 others(11): Show |
18 | HG00140.hp1 HG00423.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.518-2027_518-2026d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118398614 | ||||||
chr12:118398614 | CT | C | 18 | a0001c0001t0001g0056 a0001c0001t0001g0136 a0001c0001t0001g0146 others(15): Show |
23 | HG01081.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.518-2026delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118398614 | ||||||
chr12:118398614 | CTT | C | 15 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(12): Show |
17 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.518-2027_518-2026d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118398614 | ||||||
chr12:118398634 | C | T | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.518-2025C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398634 | |||||||
chr12:118398635 | A | C | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.518-2024A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398635 | |||||||
chr12:118398781 | C | T | 1 | a0001c0001t0025g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.518-1878C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398781 | |||||||
chr12:118398808 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.518-1851T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398808 | |||||||
chr12:118398881 | C | T | 1 | a0001c0001t0004g0072 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.518-1778C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118398881 | |||||||
chr12:118399128 | C | T | 1 | a0001c0001t0026g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.518-1531C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399128 | |||||||
chr12:118399444 | G | A | 1 | a0001c0001t0003g0266 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.518-1215G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399444 | |||||||
chr12:118399456 | C | A | 14 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 others(11): Show |
15 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.518-1203C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399456 | |||||||
chr12:118399477 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.518-1182G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399477 | |||||||
chr12:118399515 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
8 | NA18940.hp2 NA18945.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-1144A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399515 | |||||||
chr12:118399644 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.518-1015T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399644 | |||||||
chr12:118399662 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0232 |
2 | HG00280.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.518-997G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399662 | |||||||
chr12:118399802 | CGAG | C | 14 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 others(11): Show |
15 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.518-853_518-851del others(3): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr12 | 118399802 | ||||||
chr12:118399887 | G | C | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.518-772G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399887 | |||||||
chr12:118399947 | A | C | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.518-712A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118399947 | |||||||
chr12:118400055 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
8 | NA18940.hp2 NA18945.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.518-604T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400055 | |||||||
chr12:118400223 | A | G | 1 | a0001c0001t0009g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.518-436A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400223 | |||||||
chr12:118400245 | G | C | 1 | a0001c0001t0003g0267 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.518-414G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400245 | |||||||
chr12:118400295 | A | T | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.518-364A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400295 | |||||||
chr12:118400320 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(31): Show |
48 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.518-339C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400320 | |||||||
chr12:118400489 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.518-170C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400489 | |||||||
chr12:118400538 | A | G | 5 | a0001c0001t0016g0058 a0001c0001t0016g0059 a0001c0001t0016g0066 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-121A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400538 | |||||||
chr12:118400597 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.518-62A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 6/11 | chr12 | 118400597 | |||||||
chr12:118400833 | C | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+79C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118400833 | |||||||
chr12:118400974 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.613+220T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118400974 | |||||||
chr12:118401134 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.613+380C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118401134 | |||||||
chr12:118401164 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.613+410A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118401164 | |||||||
chr12:118401220 | C | G | 2 | a0001c0001t0002g0217 a0001c0001t0036g0260 |
2 | HG01358.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.613+466C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118401220 | |||||||
chr12:118401242 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.613+488C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118401242 | |||||||
chr12:118401571 | C | CT | 17 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0019 others(14): Show |
23 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.614-184dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr12 | 118401571 | ||||||
chr12:118401726 | A | G | 1 | a0001c0001t0002g0183 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.614-33A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 7/11 | chr12 | 118401726 | |||||||
chr12:118402062 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.697+58G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402062 | |||||||
chr12:118402131 | T | G | 9 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(6): Show |
13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.697+127T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402131 | |||||||
chr12:118402178 | C | CT | 7 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 others(4): Show |
9 | HG01891.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+183dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 118402178 | ||||||
chr12:118402300 | C | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.697+296C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402300 | |||||||
chr12:118402435 | C | T | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.697+431C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402435 | |||||||
chr12:118402456 | A | G | 8 | a0001c0001t0009g0020 a0001c0001t0009g0085 a0001c0001t0009g0087 others(5): Show |
9 | HG00735.hp2 HG01516.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+452A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402456 | |||||||
chr12:118402503 | C | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0082 others(8): Show |
14 | HG00438.hp2 HG00558.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.697+499C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402503 | |||||||
chr12:118402575 | C | T | 2 | a0001c0001t0009g0060 a0001c0001t0009g0062 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.697+571C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402575 | |||||||
chr12:118402630 | AAG | A | 172 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(169): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.697+629_697+630del others(2): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 118402630 | ||||||
chr12:118402652 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0023 others(113): Show |
140 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.697+648A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402652 | |||||||
chr12:118402673 | C | T | 1 | a0001c0001t0002g0233 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.697+669C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402673 | |||||||
chr12:118402691 | A | G | 322 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(319): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.697+687A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402691 | |||||||
chr12:118402704 | C | T | 130 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 others(127): Show |
150 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.697+700C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402704 | |||||||
chr12:118402761 | T | A | 1 | a0001c0001t0002g0037 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.698-651T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402761 | |||||||
chr12:118402763 | C | CT | 54 | a0001c0001t0002g0219 a0001c0001t0003g0003 a0001c0001t0003g0008 others(51): Show |
70 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.698-635dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr12 | 118402763 | ||||||
chr12:118402800 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.698-612C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118402800 | |||||||
chr12:118403109 | C | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.698-303C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118403109 | |||||||
chr12:118403117 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.698-295T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118403117 | |||||||
chr12:118403145 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.698-267T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118403145 | |||||||
chr12:118403287 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.698-125A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118403287 | |||||||
chr12:118403395 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.698-17G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 9/11 | chr12 | 118403395 | |||||||
chr12:118403528 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.803+11G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403528 | |||||||
chr12:118403569 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.803+52A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403569 | |||||||
chr12:118403605 | C | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+88C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403605 | |||||||
chr12:118403748 | G | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(223): Show |
279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.803+231G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403748 | |||||||
chr12:118403870 | T | A | 8 | a0001c0001t0002g0038 a0001c0001t0002g0234 a0001c0001t0002g0235 others(5): Show |
9 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.803+353T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403870 | |||||||
chr12:118403972 | G | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0257 a0001c0001t0002g0258 others(1): Show |
5 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.803+455G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118403972 | |||||||
chr12:118404101 | A | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+584A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404101 | |||||||
chr12:118404132 | G | A | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803+615G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404132 | |||||||
chr12:118404141 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.803+624T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404141 | |||||||
chr12:118404171 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803+654C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404171 | |||||||
chr12:118404185 | A | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
132 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.803+668A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404185 | |||||||
chr12:118404603 | T | G | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.803+1086T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404603 | |||||||
chr12:118404673 | G | A | 3 | a0001c0001t0015g0021 a0001c0001t0015g0098 a0001c0001t0015g0100 |
4 | NA18992.hp1 NA18999.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+1156G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404673 | |||||||
chr12:118404745 | C | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+1228C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118404745 | |||||||
chr12:118405022 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.803+1505C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118405022 | |||||||
chr12:118405030 | T | G | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+1513T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118405030 | |||||||
chr12:118405403 | T | C | 3 | a0001c0001t0007g0041 a0001c0001t0007g0265 a0001c0001t0025g0269 |
4 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.803+1886T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118405403 | |||||||
chr12:118405767 | T | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.803+2250T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118405767 | |||||||
chr12:118405885 | G | A | 1 | a0001c0001t0007g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.803+2368G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118405885 | |||||||
chr12:118406041 | G | A | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803+2524G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406041 | |||||||
chr12:118406095 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.803+2578A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406095 | |||||||
chr12:118406105 | G | T | 1 | a0001c0001t0042g0103 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.803+2588G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406105 | |||||||
chr12:118406192 | G | A | 3 | a0001c0001t0002g0039 a0001c0001t0002g0257 a0001c0001t0002g0259 |
4 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+2675G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406192 | |||||||
chr12:118406297 | C | T | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+2780C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406297 | |||||||
chr12:118406404 | C | G | 1 | a0001c0001t0025g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.803+2887C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406404 | |||||||
chr12:118406421 | A | C | 1 | a0001c0001t0005g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.803+2904A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406421 | |||||||
chr12:118406560 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.803+3043A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406560 | |||||||
chr12:118406707 | T | TA | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(113): Show |
137 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.803+3200dupA | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118406707 | ||||||
chr12:118406736 | T | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(108): Show |
132 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.803+3219T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406736 | |||||||
chr12:118406737 | G | A | 22 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(19): Show |
28 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.803+3220G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406737 | |||||||
chr12:118406751 | G | A | 3 | a0001c0001t0016g0058 a0001c0001t0016g0059 a0001c0001t0016g0066 |
3 | HG02451.hp1 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.803+3234G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406751 | |||||||
chr12:118406789 | T | C | 2 | a0001c0001t0007g0268 a0001c0001t0007g0282 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.803+3272T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406789 | |||||||
chr12:118406874 | C | T | 1 | a0001c0001t0012g0310 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803+3357C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406874 | |||||||
chr12:118406881 | G | A | 1 | a0001c0001t0007g0278 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.803+3364G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118406881 | |||||||
chr12:118406881 | G | GC | 19 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0120 others(16): Show |
19 | HG00544.hp1 HG00544.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.803+3371dupC | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118406881 | ||||||
chr12:118406888 | C | CA | 4 | a0001c0001t0025g0318 a0001c0001t0044g0317 a0001c0001t0045g0316 others(1): Show |
4 | HG02257.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.803+3372dupA | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118406888 | ||||||
chr12:118407135 | A | G | 1 | a0001c0001t0009g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.803+3618A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407135 | |||||||
chr12:118407280 | C | T | 3 | a0001c0001t0012g0165 a0001c0001t0012g0166 a0001c0001t0012g0167 |
3 | HG02896.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.803+3763C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407280 | |||||||
chr12:118407298 | C | G | 2 | a0001c0001t0044g0317 a0001c0001t0045g0316 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.804-3775C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407298 | |||||||
chr12:118407438 | T | C | 1 | a0001c0001t0018g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.804-3635T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407438 | |||||||
chr12:118407485 | A | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0151 |
7 | NA18962.hp2 NA18973.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-3588A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407485 | |||||||
chr12:118407511 | T | C | 3 | a0001c0001t0016g0058 a0001c0001t0016g0059 a0001c0001t0016g0066 |
3 | HG02451.hp1 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.804-3562T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407511 | |||||||
chr12:118407604 | A | G | 11 | a0001c0001t0006g0045 a0001c0001t0006g0293 a0001c0001t0006g0294 others(8): Show |
12 | HG00639.hp1 HG01099.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.804-3469A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407604 | |||||||
chr12:118407612 | C | T | 1 | a0001c0001t0045g0316 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.804-3461C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407612 | |||||||
chr12:118407720 | G | GT | 58 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0091 others(55): Show |
78 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.804-3337dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118407720 | ||||||
chr12:118407720 | G | GTT | 6 | a0001c0001t0003g0271 a0001c0001t0003g0280 a0001c0001t0003g0285 others(3): Show |
6 | HG00621.hp1 HG03139.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.804-3338_804-3337d others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118407720 | ||||||
chr12:118407720 | GT | G | 17 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0147 others(14): Show |
19 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.804-3337delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118407720 | ||||||
chr12:118407753 | C | T | 10 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0069 others(7): Show |
15 | HG00597.hp1 HG01192.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.804-3320C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407753 | |||||||
chr12:118407794 | C | G | 1 | a0001c0001t0003g0287 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.804-3279C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407794 | |||||||
chr12:118407804 | C | T | 1 | a0001c0001t0038g0201 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.804-3269C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407804 | |||||||
chr12:118407872 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.804-3201A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407872 | |||||||
chr12:118407892 | G | A | 18 | a0001c0001t0001g0024 a0001c0001t0001g0055 a0001c0001t0001g0089 others(15): Show |
19 | HG00140.hp2 HG01256.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.804-3181G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407892 | |||||||
chr12:118407987 | C | T | 14 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 others(11): Show |
15 | HG01884.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.804-3086C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118407987 | |||||||
chr12:118408047 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.804-3026C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408047 | |||||||
chr12:118408101 | A | G | 1 | a0001c0001t0044g0317 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.804-2972A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408101 | |||||||
chr12:118408178 | C | T | 1 | a0001c0001t0025g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-2895C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408178 | |||||||
chr12:118408179 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.804-2894G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408179 | |||||||
chr12:118408217 | A | G | 18 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0018 others(15): Show |
25 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.804-2856A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408217 | |||||||
chr12:118408279 | C | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-2794C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408279 | |||||||
chr12:118408319 | C | G | 3 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 |
3 | HG01884.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804-2754C>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408319 | |||||||
chr12:118408335 | G | GT | 23 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0145 others(20): Show |
25 | HG00423.hp2 HG01952.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.804-2722dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118408335 | ||||||
chr12:118408335 | GT | G | 5 | a0001c0001t0008g0014 a0001c0001t0025g0318 a0001c0001t0044g0317 others(2): Show |
7 | HG01884.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-2722delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118408335 | ||||||
chr12:118408359 | A | G | 3 | a0001c0001t0009g0060 a0001c0001t0009g0061 a0001c0001t0009g0062 |
3 | HG01884.hp1 HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.804-2714A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408359 | |||||||
chr12:118408377 | A | C | 5 | a0001c0001t0006g0293 a0001c0001t0006g0294 a0001c0001t0006g0295 others(2): Show |
5 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-2696A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408377 | |||||||
chr12:118408405 | C | T | 1 | a0001c0001t0025g0318 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.804-2668C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408405 | |||||||
chr12:118408458 | C | T | 8 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(5): Show |
10 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.804-2615C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408458 | |||||||
chr12:118408543 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-2530G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408543 | |||||||
chr12:118408593 | C | T | 2 | a0001c0001t0044g0317 a0001c0001t0045g0316 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.804-2480C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408593 | |||||||
chr12:118408679 | T | C | 1 | a0001c0001t0002g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.804-2394T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408679 | |||||||
chr12:118408691 | G | GT | 7 | a0001c0001t0001g0082 a0001c0001t0001g0152 a0001c0001t0001g0307 others(4): Show |
7 | HG03516.hp1 HG03710.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-2369dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118408691 | ||||||
chr12:118408691 | G | T | 5 | a0001c0001t0001g0136 a0001c0001t0008g0313 a0001c0001t0012g0309 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-2382G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408691 | |||||||
chr12:118408726 | G | C | 1 | a0001c0001t0002g0243 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.804-2347G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118408726 | |||||||
chr12:118409118 | C | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0208 a0001c0001t0002g0213 |
3 | HG02523.hp2 NA18946.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.804-1955C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409118 | |||||||
chr12:118409124 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.804-1949C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409124 | |||||||
chr12:118409149 | C | CT | 11 | a0001c0001t0001g0140 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
15 | HG01346.hp2 HG01884.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.804-1908dupT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118409149 | ||||||
chr12:118409149 | CT | C | 18 | a0001c0001t0002g0181 a0001c0001t0005g0046 a0001c0001t0005g0048 others(15): Show |
20 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.804-1908delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118409149 | ||||||
chr12:118409181 | T | C | 1 | a0001c0001t0034g0192 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.804-1892T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409181 | |||||||
chr12:118409204 | G | A | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-1869G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409204 | |||||||
chr12:118409226 | C | T | 1 | a0001c0001t0003g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.804-1847C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409226 | |||||||
chr12:118409308 | G | C | 3 | a0001c0001t0003g0272 a0001c0001t0003g0277 a0001c0001t0040g0292 |
3 | NA18961.hp1 NA18978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.804-1765G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409308 | |||||||
chr12:118409352 | G | A | 1 | a0001c0001t0005g0329 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804-1721G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409352 | |||||||
chr12:118409353 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG00597.hp2 NA18944.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-1720G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409353 | |||||||
chr12:118409354 | C | T | 1 | a0001c0001t0002g0033 | 2 | NA18995.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.804-1719C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409354 | |||||||
chr12:118409359 | C | A | 1 | a0001c0001t0005g0329 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804-1714C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409359 | |||||||
chr12:118409440 | C | T | 1 | a0001c0001t0004g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804-1633C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409440 | |||||||
chr12:118409501 | A | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02040.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.804-1572A>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409501 | |||||||
chr12:118409518 | TAGC | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-1552_804-1550d others(5): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118409518 | ||||||
chr12:118409549 | T | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0133 a0001c0001t0001g0139 others(2): Show |
5 | HG02080.hp2 NA19003.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.804-1524T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409549 | |||||||
chr12:118409560 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.804-1513C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409560 | |||||||
chr12:118409595 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0010g0040 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.804-1478G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409595 | |||||||
chr12:118409784 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.804-1289G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409784 | |||||||
chr12:118409847 | T | G | 14 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(11): Show |
16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.804-1226T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118409847 | |||||||
chr12:118410053 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.804-1020G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410053 | |||||||
chr12:118410054 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.804-1019C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410054 | |||||||
chr12:118410482 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0209 a0001c0001t0002g0221 |
4 | HG00438.hp1 HG02129.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.804-591G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410482 | |||||||
chr12:118410542 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-531T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410542 | |||||||
chr12:118410555 | C | CTTTATTT others(5): Show |
35 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(32): Show |
49 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.804-502_804-491dup others(12): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410555 | ||||||
chr12:118410555 | C | CTTTATTT others(9): Show |
2 | a0001c0001t0003g0270 a0001c0001t0003g0274 |
2 | NA19081.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.804-506_804-491dup others(16): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410555 | ||||||
chr12:118410555 | CTTTATTT others(18): Show |
C | 32 | a0001c0001t0004g0006 a0001c0001t0004g0009 a0001c0001t0004g0018 others(29): Show |
40 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.804-490_804-466del others(25): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410555 | ||||||
chr12:118410579 | A | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
8 | HG00642.hp2 HG01074.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-494A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410579 | |||||||
chr12:118410579 | AT | A | 18 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(15): Show |
24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.804-490delT | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410579 | ||||||
chr12:118410580 | T | A | 7 | a0001c0001t0001g0025 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
8 | HG00642.hp2 HG01074.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.804-493T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410580 | |||||||
chr12:118410580 | T | TTTATTTA others(5): Show |
11 | a0001c0001t0003g0288 a0001c0001t0003g0290 a0001c0001t0006g0045 others(8): Show |
12 | HG00639.hp1 HG00673.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.804-491_804-490ins others(12): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410580 | ||||||
chr12:118410580 | T | TTTTA | 4 | a0001c0001t0001g0107 a0001c0001t0010g0002 a0001c0001t0025g0318 others(1): Show |
5 | HG01256.hp2 HG01258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.804-465_804-462dup others(4): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410580 | ||||||
chr12:118410583 | T | A | 4 | a0001c0001t0001g0108 a0001c0001t0012g0309 a0001c0001t0012g0310 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.804-490T>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410583 | |||||||
chr12:118410584 | A | T | 3 | a0001c0001t0012g0309 a0001c0001t0012g0310 a0001c0001t0012g0311 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.804-489A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410584 | |||||||
chr12:118410585 | TTTA | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-485_804-483del others(3): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410585 | ||||||
chr12:118410589 | TTTA | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.804-481_804-479del others(3): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr12 | 118410589 | ||||||
chr12:118410617 | G | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
118 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.804-456G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410617 | |||||||
chr12:118410636 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-437G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410636 | |||||||
chr12:118410704 | C | A | 1 | a0001c0001t0041g0063 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.804-369C>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118410704 | |||||||
chr12:118411013 | G | A | 1 | a0001c0001t0039g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.804-60G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 10/11 | chr12 | 118411013 | |||||||
chr12:118411273 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0176 a0001c0001t0001g0180 others(1): Show |
5 | HG00735.hp1 HG01515.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+116T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411273 | |||||||
chr12:118411316 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0111 others(2): Show |
5 | HG02818.hp2 HG02886.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.888+159A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411316 | |||||||
chr12:118411344 | G | A | 19 | a0001c0001t0009g0020 a0001c0001t0009g0060 a0001c0001t0009g0061 others(16): Show |
21 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.888+187G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411344 | |||||||
chr12:118411349 | A | G | 4 | a0001c0001t0005g0324 a0001c0001t0005g0326 a0001c0001t0005g0327 others(1): Show |
4 | HG00323.hp1 HG02698.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+192A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411349 | |||||||
chr12:118411356 | C | T | 1 | a0001c0001t0023g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.888+199C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411356 | |||||||
chr12:118411363 | G | A | 1 | a0001c0001t0005g0323 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.888+206G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411363 | |||||||
chr12:118411398 | C | T | 1 | a0001c0001t0005g0328 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.888+241C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411398 | |||||||
chr12:118411654 | C | T | 1 | a0001c0001t0035g0189 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.888+497C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411654 | |||||||
chr12:118411665 | T | G | 48 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(45): Show |
63 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.888+508T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411665 | |||||||
chr12:118411693 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.888+536G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411693 | |||||||
chr12:118411704 | C | T | 120 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(117): Show |
153 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.888+547C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411704 | |||||||
chr12:118411997 | G | A | 2 | a0001c0001t0025g0318 a0001c0001t0046g0319 |
2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.888+840G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118411997 | |||||||
chr12:118412116 | A | T | 1 | a0001c0001t0003g0275 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.888+959A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412116 | |||||||
chr12:118412361 | G | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.888+1204G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412361 | |||||||
chr12:118412437 | G | A | 1 | a0001c0001t0046g0319 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.888+1280G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412437 | |||||||
chr12:118412525 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.888+1368C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412525 | |||||||
chr12:118412761 | T | C | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.889-1574T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412761 | |||||||
chr12:118412763 | TC | T | 13 | a0001c0001t0005g0046 a0001c0001t0005g0048 a0001c0001t0005g0320 others(10): Show |
15 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.889-1568delC | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 118412763 | ||||||
chr12:118412798 | A | G | 6 | a0001c0001t0011g0016 a0001c0001t0011g0052 a0001c0001t0011g0053 others(3): Show |
7 | HG02809.hp2 HG02818.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-1537A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412798 | |||||||
chr12:118412816 | G | T | 1 | a0001c0001t0002g0224 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.889-1519G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412816 | |||||||
chr12:118412843 | C | T | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(231): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.889-1492C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412843 | |||||||
chr12:118412902 | A | G | 2 | a0001c0001t0012g0165 a0001c0001t0012g0167 |
2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.889-1433A>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412902 | |||||||
chr12:118412945 | T | G | 1 | a0001c0001t0001g0156 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.889-1390T>G | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118412945 | |||||||
chr12:118413194 | G | T | 1 | a0001c0001t0002g0188 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.889-1141G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413194 | |||||||
chr12:118413198 | T | C | 1 | a0001c0001t0012g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.889-1137T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413198 | |||||||
chr12:118413265 | G | C | 2 | a0001c0001t0014g0168 a0001c0001t0014g0194 |
2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.889-1070G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413265 | |||||||
chr12:118413410 | C | T | 1 | a0001c0001t0007g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.889-925C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413410 | |||||||
chr12:118413420 | G | T | 1 | a0001c0001t0005g0327 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.889-915G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413420 | |||||||
chr12:118413452 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.889-883T>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413452 | |||||||
chr12:118413637 | G | T | 5 | a0001c0001t0008g0014 a0001c0001t0008g0015 a0001c0001t0008g0313 others(2): Show |
9 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-698G>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413637 | |||||||
chr12:118413690 | T | TCAATGGA others(15): Show |
1 | a0001c0001t0030g0304 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.889-644_889-623dup others(22): Show |
SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr12 | 118413690 | ||||||
chr12:118413759 | G | C | 1 | a0001c0001t0009g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.889-576G>C | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413759 | |||||||
chr12:118413815 | C | T | 1 | a0001c0001t0005g0324 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.889-520C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413815 | |||||||
chr12:118413870 | C | T | 2 | a0001c0001t0007g0268 a0001c0001t0007g0282 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.889-465C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413870 | |||||||
chr12:118413875 | C | T | 48 | a0001c0001t0003g0003 a0001c0001t0003g0008 a0001c0001t0003g0012 others(45): Show |
63 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.889-460C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118413875 | |||||||
chr12:118414053 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.889-282A>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118414053 | |||||||
chr12:118414120 | C | T | 12 | a0001c0001t0005g0046 a0001c0001t0005g0320 a0001c0001t0005g0321 others(9): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.889-215C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118414120 | |||||||
chr12:118414126 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.889-209C>T | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118414126 | |||||||
chr12:118414149 | G | A | 1 | a0001c0001t0036g0260 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.889-186G>A | SUDS3 | ENSG00000111707.12 | transcript | ENST00000543473.2 | protein_coding | 11/11 | chr12 | 118414149 |