geneid | 54550 |
---|---|
ensemblid | ENSG00000103154.10 |
hgncid | 23746 |
symbol | NECAB2 |
name | N-terminal EF-hand calcium binding protein 2 |
refseq_nuc | NM_019065.3 |
refseq_prot | NP_061938.2 |
ensembl_nuc | ENST00000305202.9 |
ensembl_prot | ENSP00000307449.4 |
mane_status | MANE Select |
chr | chr16 |
start | 83968244 |
end | 84002776 |
strand | + |
ver | v1.2 |
region | chr16:83968244-84002776 |
region5000 | chr16:83963244-84007776 |
regionname0 | NECAB2_chr16_83968244_84002776 |
regionname5000 | NECAB2_chr16_83963244_84007776 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 386 | 138 | 8 | 46 | 43 | 11 | 28 | 25 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002 | 0/0 | 386 | 113 | 38 | 10 | 58 | 1 | 6 | 44 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003 | 0/0 | 386 | 42 | 32 | 7 | 2 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004 | 0/0 | 386 | 32 | 13 | 4 | 10 | 0 | 5 | 9 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005 | 0/0 | 386 | 10 | 0 | 3 | 6 | 0 | 1 | 5 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006 | 0/0 | 386 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007 | 0/0 | 386 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0008 | 0/0 | 386 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0009 | 0/0 | 386 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0010 | 0/0 | 386 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0011 | 0/0 | 386 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0012 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0013 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0014 | 0/0 | 386 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0015 | 0/0 | 386 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0016 | 0/0 | 386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1161 | 110 | 6 | 34 | 32 | 10 | 26 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0002 | 0/0 | 1161 | 71 | 8 | 10 | 47 | 1 | 5 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0003 | 0/0 | 1161 | 36 | 25 | 0 | 11 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0004 | 0/0 | 1161 | 29 | 22 | 5 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0005 | 0/0 | 1161 | 25 | 9 | 4 | 8 | 0 | 4 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0006 | 0/0 | 1161 | 18 | 2 | 10 | 4 | 1 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0007 | 0/0 | 1161 | 9 | 0 | 1 | 7 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0008 | 0/0 | 1161 | 7 | 7 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0009 | 0/0 | 1161 | 5 | 0 | 0 | 5 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0010 | 0/0 | 1161 | 4 | 0 | 3 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0011 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0012 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0013 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0014 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0015 | 0/0 | 1161 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0016 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0017 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0018 | 0/0 | 1161 | 2 | 0 | 0 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0019 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0020 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0021 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0022 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0023 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0024 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0025 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0026 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0027 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0028 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0029 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0030 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0031 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0032 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0033 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0034 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0035 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0036 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
c0037 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 836 | 99 | 5 | 19 | 55 | 6 | 13 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0002 | 0/0 | 836 | 39 | 0 | 16 | 12 | 4 | 7 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0003 | 0/0 | 838 | 33 | 22 | 4 | 6 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0004 | 0/0 | 838 | 21 | 21 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0005 | 0/0 | 836 | 20 | 7 | 4 | 8 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0006 | 0/0 | 838 | 18 | 0 | 7 | 11 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0007 | 0/0 | 836 | 14 | 1 | 2 | 9 | 1 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0008 | 0/0 | 838 | 12 | 3 | 0 | 8 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0009 | 0/0 | 836 | 10 | 1 | 2 | 5 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0010 | 0/0 | 838 | 8 | 7 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0011 | 0/1 | 838 | 7 | 0 | 0 | 0 | 0 | 6 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0012 | 0/0 | 838 | 4 | 4 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0013 | 0/0 | 838 | 4 | 0 | 2 | 1 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0014 | 0/0 | 838 | 3 | 0 | 2 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0015 | 0/0 | 838 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0016 | 0/0 | 836 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0017 | 0/0 | 836 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0018 | 0/0 | 838 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0019 | 0/0 | 839 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0020 | 0/0 | 838 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0021 | 0/0 | 838 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0022 | 0/0 | 838 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0023 | 0/0 | 838 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0024 | 0/0 | 838 | 2 | 0 | 0 | 0 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0025 | 0/0 | 836 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0026 | 0/0 | 836 | 2 | 0 | 0 | 0 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0027 | 0/0 | 837 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0028 | 0/0 | 837 | 2 | 0 | 1 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0029 | 0/0 | 837 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0030 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0031 | 0/0 | 839 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0032 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0033 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0034 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0035 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0036 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0037 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0038 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0039 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0040 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0041 | 0/0 | 836 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0042 | 0/0 | 836 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0043 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0044 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0045 | 0/0 | 836 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0046 | 0/0 | 837 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0047 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0048 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0049 | 0/0 | 836 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0050 | 0/0 | 838 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0051 | 0/0 | 836 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0052 | 0/0 | 836 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0053 | 0/0 | 836 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0054 | 0/0 | 840 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0055 | 0/0 | 838 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0056 | 0/0 | 839 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
t0057 | 0/0 | 837 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1161 | 110 | 6 | 34 | 32 | 10 | 26 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006 | 0/0 | 1161 | 18 | 2 | 10 | 4 | 1 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0007 | 0/0 | 1161 | 9 | 0 | 1 | 7 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0033 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002 | 0/0 | 1161 | 71 | 8 | 10 | 47 | 1 | 5 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003 | 0/0 | 1161 | 36 | 25 | 0 | 11 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0011 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0020 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0026 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0029 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004 | 0/0 | 1161 | 29 | 22 | 5 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0008 | 0/0 | 1161 | 7 | 7 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0015 | 0/0 | 1161 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0016 | 0/0 | 1161 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0028 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005 | 0/0 | 1161 | 25 | 9 | 4 | 8 | 0 | 4 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0013 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0018 | 0/0 | 1161 | 2 | 0 | 0 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0036 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0037 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0009 | 0/0 | 1161 | 5 | 0 | 0 | 5 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0010 | 0/0 | 1161 | 4 | 0 | 3 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0027 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006c0012 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006c0021 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0017 | 0/0 | 1161 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0025 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0031 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0008c0014 | 0/0 | 1161 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0009c0032 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0010c0034 | 0/0 | 1161 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0011c0035 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0012c0024 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0013c0023 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0014c0022 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0015c0030 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0016c0019 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1996 | 50 | 4 | 13 | 14 | 6 | 12 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0002 | 0/0 | 1996 | 28 | 0 | 9 | 11 | 3 | 5 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0005 | 0/0 | 1996 | 2 | 0 | 0 | 1 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0006 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0007 | 0/0 | 1996 | 3 | 0 | 1 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0009 | 0/0 | 1996 | 6 | 1 | 1 | 2 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0011 | 0/1 | 1998 | 5 | 0 | 0 | 0 | 0 | 4 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0014 | 0/0 | 1998 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0016 | 0/0 | 1996 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0027 | 0/0 | 1997 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0028 | 0/0 | 1997 | 2 | 0 | 1 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0029 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0048 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0049 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0050 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0051 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0052 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0053 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0056 | 0/0 | 1999 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0001t0057 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006t0002 | 0/0 | 1996 | 8 | 0 | 6 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006t0003 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006t0005 | 0/0 | 1996 | 3 | 1 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006t0007 | 0/0 | 1996 | 5 | 0 | 1 | 3 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0006t0042 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0007t0001 | 0/0 | 1996 | 5 | 0 | 0 | 5 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0007t0002 | 0/0 | 1996 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0007t0006 | 0/0 | 1998 | 3 | 0 | 1 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0001c0033t0009 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0001 | 0/0 | 1996 | 41 | 1 | 6 | 34 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0003 | 0/0 | 1998 | 6 | 4 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0006 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0007 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0008 | 0/0 | 1998 | 7 | 0 | 0 | 6 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0009 | 0/0 | 1996 | 3 | 0 | 0 | 3 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0011 | 0/0 | 1998 | 2 | 0 | 0 | 0 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0013 | 0/0 | 1998 | 3 | 0 | 1 | 1 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0019 | 0/0 | 1999 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0024 | 0/0 | 1998 | 2 | 0 | 0 | 0 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0029 | 0/0 | 1997 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0047 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0002t0055 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0003 | 0/0 | 1998 | 13 | 7 | 0 | 6 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0004 | 0/0 | 1998 | 9 | 9 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0007 | 0/0 | 1996 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0008 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0010 | 0/0 | 1998 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0012 | 0/0 | 1998 | 4 | 4 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0022 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0031 | 0/0 | 1999 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0036 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0003t0044 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0011t0004 | 0/0 | 1998 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0020t0003 | 0/0 | 1998 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0026t0032 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0002c0029t0010 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0003 | 0/0 | 1998 | 8 | 6 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0004 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0007 | 0/0 | 1996 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0008 | 0/0 | 1998 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0010 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0013 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0021 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0022 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0023 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0025 | 0/0 | 1996 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0030 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0033 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0037 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0039 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0004t0040 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0008t0004 | 0/0 | 1998 | 7 | 7 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0015t0018 | 0/0 | 1998 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0016t0020 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0003c0028t0034 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0002 | 0/0 | 1996 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0005 | 0/0 | 1996 | 14 | 5 | 2 | 7 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0007 | 0/0 | 1996 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0010 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0016 | 0/0 | 1996 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0026 | 0/0 | 1996 | 2 | 0 | 0 | 0 | 0 | 2 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0027 | 0/0 | 1997 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0041 | 0/0 | 1996 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0043 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0005t0046 | 0/0 | 1997 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0013t0017 | 0/0 | 1996 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0018t0001 | 0/0 | 1996 | 2 | 0 | 0 | 1 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0036t0005 | 0/0 | 1996 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0004c0037t0006 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0009t0006 | 0/0 | 1998 | 4 | 0 | 0 | 4 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0009t0054 | 0/0 | 2000 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0010t0006 | 0/0 | 1998 | 4 | 0 | 3 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0005c0027t0045 | 0/0 | 1996 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006c0012t0003 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006c0012t0015 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0006c0021t0015 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0017t0006 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0017t0014 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0025t0006 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0007c0031t0006 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0008c0014t0003 | 0/0 | 1998 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0008c0014t0038 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0009c0032t0008 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0010c0034t0002 | 0/0 | 1996 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0011c0035t0001 | 0/0 | 1996 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0012c0024t0004 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0013c0023t0010 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0014c0022t0035 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0015c0030t0003 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
a0016c0019t0006 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | copy fasta | chr16 | 83963244 | 84007776 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0007g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0007g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0009g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0011g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0011g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0011g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0011g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0014g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0014g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0016g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0027g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0028g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0028g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0029g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0048g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0049g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0050g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0051g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0052g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0053g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0056g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0001t0057g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0007g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0007g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0006t0042g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0007t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0001c0033t0009g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0007g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0009g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0011g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0013g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0013g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0013g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0019g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0024g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0024g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0029g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0047g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0002t0055g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0007g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0010g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0012g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0012g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0012g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0022g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0031g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0036g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0003t0044g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0011t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0011t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0011t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0020t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0026t0032g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0002c0029t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0007g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0021g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0021g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0022g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0023g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0023g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0025g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0030g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0033g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0037g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0039g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0004t0040g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0008t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0015t0018g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0015t0018g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0015t0018g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0016t0020g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0016t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0003c0028t0034g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0026g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0026g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0027g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0041g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0043g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0005t0046g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0013t0017g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0013t0017g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0013t0017g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0018t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0018t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0036t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0004c0037t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0009t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0009t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0009t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0009t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0009t0054g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0010t0006g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0010t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0010t0006g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0010t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0005c0027t0045g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0006c0012t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0006c0012t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0006c0012t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0006c0021t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0007c0017t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0007c0017t0014g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0007c0025t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0007c0031t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0008c0014t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0008c0014t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0008c0014t0038g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0009c0032t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0010c0034t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0011c0035t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0012c0024t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0013c0023t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0014c0022t0035g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0015c0030t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
a0016c0019t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0042 | EUR | GBR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00099 | hp2 | a0010 | c0034 | t0002 | g0259 | EUR | GBR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0286 | EUR | GBR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | FIN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00423 | hp1 | a0002 | c0002 | t0013 | g0340 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00423 | hp2 | a0001 | c0001 | t0053 | g0188 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00609 | hp1 | a0001 | c0001 | t0009 | g0140 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00642 | hp2 | a0001 | c0006 | t0005 | g0275 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00738 | hp1 | a0001 | c0001 | t0007 | g0262 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00738 | hp2 | a0001 | c0006 | t0005 | g0277 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG00741 | hp2 | a0004 | c0005 | t0005 | g0269 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01070 | hp2 | a0001 | c0001 | t0052 | g0166 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01081 | hp1 | a0001 | c0033 | t0009 | g0201 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01081 | hp2 | a0001 | c0007 | t0006 | g0215 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01099 | hp1 | a0005 | c0010 | t0006 | g0088 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0172 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01167 | hp1 | a0003 | c0004 | t0025 | g0223 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01167 | hp2 | a0004 | c0005 | t0002 | g0019 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01168 | hp1 | a0001 | c0001 | t0051 | g0202 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01168 | hp2 | a0001 | c0001 | t0014 | g0301 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01169 | hp1 | a0001 | c0001 | t0014 | g0300 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01169 | hp2 | a0003 | c0004 | t0025 | g0222 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01175 | hp1 | a0004 | c0005 | t0027 | g0020 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01175 | hp2 | a0001 | c0001 | t0028 | g0153 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01192 | hp1 | a0001 | c0001 | t0027 | g0106 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0089 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0173 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01243 | hp2 | a0003 | c0004 | t0003 | g0035 | AMR | PUR | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01255 | hp1 | a0001 | c0006 | t0042 | g0333 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01255 | hp2 | a0003 | c0004 | t0003 | g0248 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01256 | hp2 | a0001 | c0006 | t0002 | g0023 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01257 | hp2 | a0003 | c0015 | t0018 | g0204 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01258 | hp1 | a0003 | c0015 | t0018 | g0205 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01258 | hp2 | a0001 | c0006 | t0002 | g0022 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01261 | hp2 | a0001 | c0001 | t0056 | g0114 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01346 | hp2 | a0001 | c0001 | t0049 | g0103 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01358 | hp1 | a0001 | c0001 | t0050 | g0098 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01361 | hp2 | a0001 | c0006 | t0002 | g0028 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01433 | hp1 | a0003 | c0004 | t0013 | g0220 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01433 | hp2 | a0004 | c0005 | t0005 | g0240 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01496 | hp1 | a0001 | c0006 | t0007 | g0332 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01496 | hp2 | a0001 | c0001 | t0009 | g0096 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01884 | hp1 | a0003 | c0004 | t0023 | g0034 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01884 | hp2 | a0002 | c0003 | t0004 | g0230 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01891 | hp1 | a0002 | c0002 | t0019 | g0254 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01891 | hp2 | a0003 | c0028 | t0034 | g0289 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01928 | hp1 | a0005 | c0010 | t0006 | g0087 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01943 | hp1 | a0005 | c0010 | t0006 | g0111 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01943 | hp2 | a0001 | c0006 | t0002 | g0025 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01975 | hp1 | a0013 | c0023 | t0010 | g0321 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0080 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01993 | hp2 | a0001 | c0006 | t0002 | g0024 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02004 | hp2 | a0002 | c0002 | t0006 | g0079 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02015 | hp1 | a0001 | c0007 | t0001 | g0142 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02027 | hp1 | a0001 | c0007 | t0001 | g0156 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02027 | hp2 | a0002 | c0002 | t0008 | g0062 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02055 | hp1 | a0003 | c0004 | t0008 | g0225 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02055 | hp2 | a0002 | c0003 | t0031 | g0310 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02056 | hp2 | a0002 | c0002 | t0029 | g0029 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02071 | hp1 | a0001 | c0007 | t0001 | g0233 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02074 | hp2 | a0004 | c0005 | t0043 | g0303 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02080 | hp2 | a0001 | c0007 | t0006 | g0169 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02083 | hp1 | a0002 | c0002 | t0008 | g0093 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02132 | hp1 | a0003 | c0004 | t0007 | g0276 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02132 | hp2 | a0011 | c0035 | t0001 | g0168 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02135 | hp1 | a0001 | c0006 | t0007 | g0211 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02135 | hp2 | a0001 | c0007 | t0001 | g0149 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02145 | hp1 | a0003 | c0008 | t0004 | g0015 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02145 | hp2 | a0002 | c0003 | t0012 | g0238 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02155 | hp1 | a0002 | c0002 | t0008 | g0016 | EAS | CDX | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CDX | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02165 | hp1 | a0005 | c0009 | t0006 | g0148 | EAS | CDX | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02165 | hp2 | a0002 | c0002 | t0008 | g0135 | EAS | CDX | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02257 | hp2 | a0008 | c0014 | t0038 | g0236 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02258 | hp1 | a0002 | c0003 | t0010 | g0330 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02258 | hp2 | a0003 | c0004 | t0003 | g0249 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02280 | hp1 | a0003 | c0004 | t0037 | g0313 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02280 | hp2 | a0003 | c0008 | t0004 | g0017 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02300 | hp1 | a0016 | c0019 | t0006 | g0112 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02300 | hp2 | a0001 | c0006 | t0002 | g0026 | AMR | PEL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0318 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02451 | hp2 | a0002 | c0003 | t0004 | g0260 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02523 | hp2 | a0001 | c0001 | t0048 | g0006 | EAS | KHV | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02572 | hp1 | a0003 | c0008 | t0004 | g0210 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02572 | hp2 | a0012 | c0024 | t0004 | g0331 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02602 | hp1 | a0004 | c0005 | t0046 | g0273 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02602 | hp2 | a0002 | c0020 | t0003 | g0228 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02615 | hp1 | a0006 | c0021 | t0015 | g0008 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02615 | hp2 | a0003 | c0004 | t0004 | g0257 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02622 | hp1 | a0003 | c0008 | t0004 | g0036 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02622 | hp2 | a0002 | c0026 | t0032 | g0012 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02630 | hp1 | a0003 | c0008 | t0004 | g0208 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02630 | hp2 | a0004 | c0005 | t0016 | g0010 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02647 | hp1 | a0006 | c0012 | t0003 | g0312 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02647 | hp2 | a0003 | c0004 | t0022 | g0295 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02683 | hp1 | a0001 | c0001 | t0011 | g0345 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02698 | hp1 | a0001 | c0001 | t0011 | g0344 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02698 | hp2 | a0001 | c0001 | t0028 | g0091 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02717 | hp1 | a0002 | c0003 | t0004 | g0315 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02717 | hp2 | a0004 | c0005 | t0005 | g0246 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02723 | hp1 | a0002 | c0003 | t0004 | g0337 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02723 | hp2 | a0003 | c0004 | t0010 | g0235 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0120 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02735 | hp2 | a0001 | c0006 | t0002 | g0037 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02809 | hp1 | a0002 | c0002 | t0019 | g0175 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02809 | hp2 | a0003 | c0004 | t0033 | g0297 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02818 | hp1 | a0002 | c0003 | t0012 | g0327 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02818 | hp2 | a0002 | c0003 | t0004 | g0261 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02886 | hp1 | a0015 | c0030 | t0003 | g0317 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02886 | hp2 | a0002 | c0003 | t0003 | g0311 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02895 | hp1 | a0002 | c0003 | t0012 | g0326 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02895 | hp2 | a0004 | c0005 | t0010 | g0237 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02896 | hp1 | a0004 | c0005 | t0005 | g0180 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02896 | hp2 | a0002 | c0011 | t0004 | g0293 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02897 | hp1 | a0002 | c0011 | t0004 | g0292 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02897 | hp2 | a0002 | c0003 | t0012 | g0325 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02922 | hp1 | a0003 | c0004 | t0039 | g0242 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02922 | hp2 | a0003 | c0004 | t0003 | g0252 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02965 | hp1 | a0002 | c0029 | t0010 | g0328 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02965 | hp2 | a0008 | c0014 | t0003 | g0194 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02970 | hp1 | a0006 | c0012 | t0015 | g0014 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02970 | hp2 | a0003 | c0004 | t0030 | g0329 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02976 | hp1 | a0002 | c0002 | t0047 | g0030 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02976 | hp2 | a0002 | c0003 | t0003 | g0224 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03017 | hp1 | a0005 | c0027 | t0045 | g0288 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03017 | hp2 | a0002 | c0002 | t0008 | g0031 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03041 | hp1 | a0002 | c0003 | t0003 | g0296 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03041 | hp2 | a0002 | c0003 | t0010 | g0221 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0176 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03098 | hp2 | a0002 | c0003 | t0004 | g0316 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03130 | hp1 | a0002 | c0003 | t0004 | g0314 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03130 | hp2 | a0003 | c0004 | t0021 | g0239 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03139 | hp1 | a0003 | c0004 | t0003 | g0245 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03139 | hp2 | a0003 | c0016 | t0020 | g0032 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03195 | hp1 | a0002 | c0003 | t0004 | g0232 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03195 | hp2 | a0002 | c0011 | t0004 | g0291 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03209 | hp1 | a0004 | c0013 | t0017 | g0219 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03209 | hp2 | a0001 | c0001 | t0016 | g0258 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03225 | hp1 | a0002 | c0003 | t0003 | g0264 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03225 | hp2 | a0003 | c0008 | t0004 | g0011 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03453 | hp1 | a0001 | c0006 | t0003 | g0336 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03453 | hp2 | a0004 | c0036 | t0005 | g0214 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03486 | hp1 | a0003 | c0016 | t0020 | g0216 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03486 | hp2 | a0003 | c0008 | t0004 | g0209 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03490 | hp1 | a0004 | c0005 | t0026 | g0281 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0137 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03491 | hp1 | a0002 | c0002 | t0024 | g0323 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0343 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03492 | hp1 | a0002 | c0002 | t0024 | g0324 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03492 | hp2 | a0004 | c0005 | t0026 | g0280 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03516 | hp1 | a0001 | c0006 | t0005 | g0256 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03516 | hp2 | a0002 | c0003 | t0003 | g0229 | AFR | ESN | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03540 | hp1 | a0004 | c0005 | t0016 | g0009 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03540 | hp2 | a0002 | c0003 | t0003 | g0265 | AFR | GWD | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03579 | hp1 | a0003 | c0004 | t0008 | g0226 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03688 | hp2 | a0001 | c0007 | t0002 | g0138 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03710 | hp1 | a0002 | c0002 | t0011 | g0165 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03710 | hp2 | a0001 | c0001 | t0057 | g0108 | SAS | PJL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | BEB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | BEB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03942 | hp2 | a0002 | c0002 | t0011 | g0163 | SAS | BEB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04199 | hp1 | a0004 | c0018 | t0001 | g0302 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04199 | hp2 | a0001 | c0001 | t0011 | g0342 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04204 | hp2 | a0004 | c0005 | t0041 | g0274 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0322 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18522 | hp1 | a0006 | c0012 | t0015 | g0013 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18522 | hp2 | a0003 | c0004 | t0003 | g0243 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18747 | hp1 | a0002 | c0003 | t0036 | g0007 | EAS | CHB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18747 | hp2 | a0001 | c0006 | t0007 | g0212 | EAS | CHB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0255 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18906 | hp2 | a0003 | c0004 | t0003 | g0247 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18944 | hp2 | a0005 | c0009 | t0006 | g0038 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18946 | hp1 | a0002 | c0003 | t0008 | g0027 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18950 | hp1 | a0004 | c0018 | t0001 | g0040 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18950 | hp2 | a0002 | c0003 | t0044 | g0309 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18953 | hp1 | a0004 | c0005 | t0005 | g0270 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18954 | hp1 | a0002 | c0003 | t0003 | g0307 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18959 | hp1 | a0001 | c0006 | t0007 | g0213 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18961 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18962 | hp1 | a0002 | c0003 | t0007 | g0298 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18962 | hp2 | a0007 | c0017 | t0006 | g0109 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18969 | hp1 | a0001 | c0006 | t0002 | g0158 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0285 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18970 | hp2 | a0009 | c0032 | t0008 | g0125 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18971 | hp2 | a0004 | c0005 | t0005 | g0278 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18977 | hp1 | a0004 | c0005 | t0005 | g0263 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18977 | hp2 | a0007 | c0031 | t0006 | g0064 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18980 | hp1 | a0002 | c0003 | t0007 | g0308 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18984 | hp1 | a0002 | c0002 | t0008 | g0341 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18986 | hp1 | a0005 | c0009 | t0006 | g0039 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18990 | hp2 | a0002 | c0002 | t0009 | g0185 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18991 | hp1 | a0002 | c0002 | t0055 | g0001 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18991 | hp2 | a0005 | c0009 | t0054 | g0146 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18994 | hp2 | a0005 | c0009 | t0006 | g0147 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19002 | hp2 | a0001 | c0001 | t0009 | g0002 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19004 | hp1 | a0002 | c0003 | t0003 | g0306 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19004 | hp2 | a0002 | c0002 | t0009 | g0139 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19005 | hp1 | a0001 | c0007 | t0001 | g0141 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19010 | hp2 | a0007 | c0017 | t0014 | g0287 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19030 | hp1 | a0008 | c0014 | t0003 | g0320 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0253 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19043 | hp1 | a0003 | c0004 | t0021 | g0244 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19043 | hp2 | a0004 | c0013 | t0017 | g0217 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19057 | hp1 | a0002 | c0003 | t0003 | g0319 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19057 | hp2 | a0002 | c0002 | t0007 | g0299 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19064 | hp1 | a0002 | c0002 | t0008 | g0069 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19066 | hp1 | a0002 | c0003 | t0003 | g0304 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19066 | hp2 | a0001 | c0007 | t0006 | g0066 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19068 | hp1 | a0001 | c0001 | t0029 | g0134 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19068 | hp2 | a0014 | c0022 | t0035 | g0305 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19070 | hp1 | a0005 | c0010 | t0006 | g0113 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19070 | hp2 | a0007 | c0025 | t0006 | g0157 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19074 | hp1 | a0004 | c0005 | t0005 | g0283 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19079 | hp1 | a0004 | c0037 | t0006 | g0145 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19079 | hp2 | a0004 | c0005 | t0005 | g0271 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19081 | hp2 | a0004 | c0005 | t0005 | g0268 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19082 | hp1 | a0004 | c0005 | t0005 | g0272 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19083 | hp1 | a0002 | c0003 | t0003 | g0335 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19089 | hp1 | a0003 | c0004 | t0007 | g0282 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19240 | hp1 | a0003 | c0004 | t0008 | g0227 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA19240 | hp2 | a0003 | c0004 | t0010 | g0234 | AFR | YRI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20129 | hp1 | a0002 | c0003 | t0010 | g0334 | AFR | ASW | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20129 | hp2 | a0003 | c0004 | t0040 | g0018 | AFR | ASW | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20752 | hp1 | a0002 | c0002 | t0013 | g0118 | EUR | TSI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20752 | hp2 | a0001 | c0006 | t0007 | g0338 | EUR | TSI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20805 | hp1 | a0003 | c0015 | t0018 | g0203 | EUR | TSI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | GIH | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG01123 | hp2 | a0002 | c0002 | t0013 | g0104 | AMR | CLM | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02109 | hp1 | a0003 | c0004 | t0023 | g0033 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02109 | hp2 | a0004 | c0005 | t0005 | g0251 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02486 | hp1 | a0003 | c0004 | t0003 | g0250 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02486 | hp2 | a0004 | c0005 | t0005 | g0241 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02559 | hp1 | a0002 | c0003 | t0003 | g0266 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG02559 | hp2 | a0002 | c0003 | t0022 | g0231 | AFR | ACB | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03471 | hp1 | a0004 | c0013 | t0017 | g0218 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG03471 | hp2 | a0002 | c0003 | t0004 | g0267 | AFR | MSL | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
HG06807 | hp2 | a0004 | c0005 | t0005 | g0279 | AFR | USA | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA18955 | hp2 | a0002 | c0002 | t0009 | g0186 | EAS | JPT | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | USA | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
NA21309 | hp2 | a0004 | c0005 | t0007 | g0339 | AFR | LWK | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0200 | REF | REF | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0097 | REF | REF | NECAB2_chr16_83963244_84007776 | NECAB2 | chr16 | 83963244 | 84007776 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:83968826
|
G | C | 1 | a0016 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.178G>C | p.Gly60Arg | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 583/1996 | 178/1161 | 60/386 | chr16 | 83968826 | ||
chr16:83994330
|
G | A | 1 | a0015 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.625G>A | p.Ala209Thr | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/13 | 1030/1996 | 625/1161 | 209/386 | chr16 | 83994330 | ||
chr16:83994361
|
C | T | 1 | a0008 | 3 | HG02257.hp2 HG02965.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.656C>T | p.Pro219Leu | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/13 | 1061/1996 | 656/1161 | 219/386 | chr16 | 83994361 | ||
chr16:83994402
|
G | A | 1 | a0014 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.697G>A | p.Gly233Ser | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/13 | 1102/1996 | 697/1161 | 233/386 | chr16 | 83994402 | ||
chr16:83994409
|
C | G | 6 | a0003a0004a0005others(3): Show | 92 | HG00741.hp2 HG01099.hp1 HG01167.hp1 others(89): Show |
missense_variant | MODERATE | c.704C>G | p.Thr235Ser | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/13 | 1109/1996 | 704/1161 | 235/386 | chr16 | 83994409 | ||
chr16:83994659
|
G | A | 1 | a0013 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.766G>A | p.Ala256Thr | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/13 | 1171/1996 | 766/1161 | 256/386 | chr16 | 83994659 | ||
chr16:83994671
|
G | C | 1 | a0012 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.778G>C | p.Gly260Arg | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/13 | 1183/1996 | 778/1161 | 260/386 | chr16 | 83994671 | ||
chr16:83997217
|
C | T | 1 | a0011 | 1 | HG02132.hp2 | missense_variant&splice_region_variant | MODERATE | c.797C>T | p.Ala266Val | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/13 | 1202/1996 | 797/1161 | 266/386 | chr16 | 83997217 | ||
chr16:83998266
|
A | G | 1 | a0010 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.911A>G | p.Asp304Gly | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1316/1996 | 911/1161 | 304/386 | chr16 | 83998266 | ||
chr16:83998279
|
G | C | 4 | a0005a0007a0009others(1): Show | 16 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(13): Show |
missense_variant | MODERATE | c.924G>C | p.Gln308His | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1329/1996 | 924/1161 | 308/386 | chr16 | 83998279 | ||
chr16:83998295
|
A | G | 1 | a0006 | 4 | HG02615.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.940A>G | p.Thr314Ala | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1345/1996 | 940/1161 | 314/386 | chr16 | 83998295 | ||
chr16:84001841
|
C | G | 10 | a0002a0003a0006others(7): Show | 168 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(165): Show |
missense_variant | MODERATE | c.1057C>G | p.Leu353Val | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/13 | 1462/1996 | 1057/1161 | 353/386 | chr16 | 84001841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:83978499
|
T | C | 20 | a0001c0006a0002c0003a0002c0011others(17): Show | 139 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(136): Show |
synonymous_variant | LOW | c.282T>C | p.Leu94Leu | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/13 | 687/1996 | 282/1161 | 94/386 | chr16 | 83978499 | ||
chr16:83978532
|
G | C | 1 | a0002c0020 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.315G>C | p.Thr105Thr | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/13 | 720/1996 | 315/1161 | 105/386 | chr16 | 83978532 | ||
chr16:83990595
|
G | A | 1 | a0006c0021 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.561G>A | p.Ala187Ala | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/13 | 966/1996 | 561/1161 | 187/386 | chr16 | 83990595 | ||
chr16:83994401
|
A | G | 1 | a0002c0029 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.696A>G | p.Gln232Gln | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/13 | 1101/1996 | 696/1161 | 232/386 | chr16 | 83994401 | ||
chr16:83998276
|
C | T | 2 | a0003c0016a0004c0013 | 5 | HG03139.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
synonymous_variant | LOW | c.921C>T | p.Arg307Arg | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1326/1996 | 921/1161 | 307/386 | chr16 | 83998276 | ||
chr16:83998300
|
C | A | 2 | a0002c0026a0004c0036 | 2 | HG02622.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.945C>A | p.Gly315Gly | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1350/1996 | 945/1161 | 315/386 | chr16 | 83998300 | ||
chr16:83998300
|
C | T | 1 | a0001c0033 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.945C>T | p.Gly315Gly | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/13 | 1350/1996 | 945/1161 | 315/386 | chr16 | 83998300 | ||
chr16:84001825
|
G | A | 2 | a0002c0011a0003c0008 | 10 | HG02145.hp1 HG02280.hp2 HG02572.hp1 others(7): Show |
splice_region_variant&synonymous_variant | LOW | c.1041G>A | p.Arg347Arg | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/13 | 1446/1996 | 1041/1161 | 347/386 | chr16 | 84001825 | ||
chr16:84001852
|
G | A | 1 | a0003c0028 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1068G>A | p.Ala356Ala | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/13 | 1473/1996 | 1068/1161 | 356/386 | chr16 | 84001852 | ||
chr16:84001903
|
G | A | 1 | a0011c0035 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.1119G>A | p.Arg373Arg | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/13 | 1524/1996 | 1119/1161 | 373/386 | chr16 | 84001903 | ||
chr16:84001909
|
G | A | 5 | a0001c0007a0004c0037a0005c0009others(2): Show | 18 | HG01081.hp2 HG02015.hp1 HG02027.hp1 others(15): Show |
synonymous_variant | LOW | c.1125G>A | p.Leu375Leu | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/13 | 1530/1996 | 1125/1161 | 375/386 | chr16 | 84001909 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:83968245
|
T | C | 63 | a0001c0001t0005a0001c0001t0007a0001c0001t0014others(60): Show | 146 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(143): Show |
5_prime_UTR_variant | MODIFIER | c.-404T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 404 | chr16 | 83968245 | |||||
chr16:83968353
|
C | T | 1 | a0004c0013t0017 | 3 | HG03209.hp1 HG03471.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-296C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 296 | chr16 | 83968353 | |||||
chr16:83968356
|
C | T | 1 | a0002c0002t0047 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-293C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 293 | chr16 | 83968356 | |||||
chr16:83968373
|
C | A | 1 | a0003c0004t0030 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-276C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 276 | chr16 | 83968373 | |||||
chr16:83968494
|
C | A | 1 | a0001c0001t0048 | 1 | HG02523.hp2 | 5_prime_UTR_variant | MODIFIER | c.-155C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 155 | chr16 | 83968494 | |||||
chr16:83968528
|
C | CG | 7 | a0001c0001t0029a0001c0001t0056a0001c0001t0057others(4): Show | 7 | HG01261.hp2 HG02056.hp2 HG02602.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-116dupG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 115 | INFO_REALIGN_3_PRIME | chr16 | 83968528 | ||||
chr16:83968567
|
G | A | 1 | a0001c0001t0049 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 82 | chr16 | 83968567 | |||||
chr16:83968573
|
A | AG | 7 | a0001c0001t0027a0001c0001t0028a0002c0002t0019others(4): Show | 9 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-71dupG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/13 | 70 | INFO_REALIGN_3_PRIME | chr16 | 83968573 | ||||
chr16:84002360
|
G | A | 1 | a0002c0026t0032 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 14 | chr16 | 84002360 | |||||
chr16:84002394
|
T | G | 2 | a0003c0004t0033a0003c0016t0020 | 3 | HG02809.hp2 HG03139.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*48T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 48 | chr16 | 84002394 | |||||
chr16:84002406
|
C | CCT | 64 | a0001c0001t0006a0001c0001t0011a0001c0001t0014others(61): Show | 143 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*60_*61insCT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 61 | chr16 | 84002406 | |||||
chr16:84002407
|
G | A | 1 | a0002c0003t0012 | 4 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*61G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 61 | chr16 | 84002407 | |||||
chr16:84002431
|
G | C | 1 | a0003c0004t0021 | 2 | HG03130.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*85G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 85 | chr16 | 84002431 | |||||
chr16:84002432
|
T | G | 1 | a0003c0015t0018 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 86 | chr16 | 84002432 | |||||
chr16:84002434
|
C | T | 2 | a0006c0012t0015a0006c0021t0015 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*88C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 88 | chr16 | 84002434 | |||||
chr16:84002549
|
T | C | 1 | a0003c0016t0020 | 2 | HG03139.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*203T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 203 | chr16 | 84002549 | |||||
chr16:84002550
|
G | C | 2 | a0002c0003t0022a0003c0004t0022 | 2 | HG02559.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*204G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 204 | chr16 | 84002550 | |||||
chr16:84002557
|
C | G | 2 | a0001c0001t0016a0004c0005t0016 | 3 | HG02630.hp2 HG03209.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*211C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 211 | chr16 | 84002557 | |||||
chr16:84002574
|
C | T | 1 | a0004c0005t0026 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 228 | chr16 | 84002574 | |||||
chr16:84002575
|
G | A | 2 | a0003c0028t0034a0014c0022t0035 | 2 | HG01891.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*229G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 229 | chr16 | 84002575 | |||||
chr16:84002597
|
T | A | 1 | a0001c0001t0051 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*251T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 251 | chr16 | 84002597 | |||||
chr16:84002622
|
T | C | 84 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(81): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*276T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 276 | chr16 | 84002622 | |||||
chr16:84002651
|
A | C | 1 | a0005c0027t0045 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 305 | chr16 | 84002651 | |||||
chr16:84002673
|
C | T | 3 | a0002c0003t0022a0003c0004t0022a0003c0004t0040 | 3 | HG02559.hp2 HG02647.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*327C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 327 | chr16 | 84002673 | |||||
chr16:84002689
|
C | T | 22 | a0001c0006t0003a0002c0002t0003a0002c0002t0008others(19): Show | 59 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*343C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 343 | chr16 | 84002689 | |||||
chr16:84002698
|
A | T | 1 | a0003c0004t0039 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 352 | chr16 | 84002698 | |||||
chr16:84002720
|
A | G | 34 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(31): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*374A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 374 | chr16 | 84002720 | |||||
chr16:84002725
|
G | T | 2 | a0001c0001t0053a0004c0005t0043 | 2 | HG00423.hp2 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 379 | chr16 | 84002725 | |||||
chr16:84002734
|
C | G | 1 | a0003c0004t0037 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 388 | chr16 | 84002734 | |||||
chr16:84002744
|
G | A | 32 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(29): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*398G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 398 | chr16 | 84002744 | |||||
chr16:84002751
|
C | T | 1 | a0001c0001t0052 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*405C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 405 | chr16 | 84002751 | |||||
chr16:84002752
|
G | A | 31 | a0001c0006t0003a0002c0002t0003a0002c0002t0008others(28): Show | 88 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*406G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 406 | chr16 | 84002752 | |||||
chr16:84002762
|
C | G | 2 | a0002c0002t0047a0003c0016t0020 | 3 | HG02976.hp1 HG03139.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 13/13 | 416 | chr16 | 84002762 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:83968867
|
G | A | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201+18G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83968867 | ||||||
chr16:83968912
|
C | T | 6 | a0001c0001t0001g0347a0001c0001t0002g0346a0001c0001t0009g0343others(3): Show | 6 | HG02683.hp1 HG02698.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+63C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83968912 | ||||||
chr16:83968925
|
C | G | 2 | a0002c0002t0008g0341a0002c0002t0013g0340 | 2 | HG00423.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.201+76C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83968925 | ||||||
chr16:83968939
|
C | G | 44 | a0001c0001t0007g0322a0001c0001t0014g0300a0001c0001t0014g0301others(41): Show | 44 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.201+90C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83968939 | ||||||
chr16:83969029
|
T | A | 2 | a0004c0005t0016g0009a0004c0005t0016g0010 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.201+180T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969029 | ||||||
chr16:83969050
|
G | C | 51 | a0001c0001t0007g0322a0001c0001t0014g0300a0001c0001t0014g0301others(48): Show | 51 | HG01168.hp2 HG01169.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.201+201G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969050 | ||||||
chr16:83969131
|
C | G | 1 | a0004c0005t0007g0339 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.201+282C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969131 | ||||||
chr16:83969165
|
A | T | 3 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297 | 3 | HG02647.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.201+316A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969165 | ||||||
chr16:83969179
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.201+330C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969179 | ||||||
chr16:83969186
|
C | T | 3 | a0002c0011t0004g0291a0002c0011t0004g0292a0002c0011t0004g0293 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.201+337C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969186 | ||||||
chr16:83969204
|
C | G | 1 | a0002c0002t0001g0290 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.201+355C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969204 | ||||||
chr16:83969285
|
A | C | 59 | a0001c0001t0005g0284a0001c0001t0005g0286a0001c0001t0007g0262others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.201+436A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969285 | ||||||
chr16:83969364
|
G | A | 1 | a0003c0004t0040g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.201+515G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969364 | ||||||
chr16:83969373
|
A | C | 1 | a0003c0008t0004g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.201+524A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969373 | ||||||
chr16:83969418
|
A | G | 1 | a0001c0006t0007g0338 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.201+569A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969418 | ||||||
chr16:83969542
|
G | A | 3 | a0001c0001t0001g0021a0004c0005t0002g0019a0004c0005t0027g0020 | 3 | HG00280.hp2 HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.201+693G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969542 | ||||||
chr16:83969674
|
CGGA | C | 7 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(4): Show | 7 | HG01256.hp2 HG01258.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.201+835_201+837del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 83969674 | |||||
chr16:83969697
|
C | G | 2 | a0001c0006t0003g0336a0002c0003t0004g0337 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.201+848C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969697 | ||||||
chr16:83969863
|
G | C | 1 | a0002c0002t0029g0029 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.201+1014G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969863 | ||||||
chr16:83969944
|
G | A | 1 | a0002c0002t0047g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.201+1095G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969944 | ||||||
chr16:83969971
|
C | T | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201+1122C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969971 | ||||||
chr16:83969978
|
C | T | 1 | a0001c0007t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.201+1129C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969978 | ||||||
chr16:83969989
|
A | G | 1 | a0003c0028t0034g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.201+1140A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83969989 | ||||||
chr16:83970002
|
C | T | 1 | a0002c0003t0003g0335 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.201+1153C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970002 | ||||||
chr16:83970018
|
C | T | 2 | a0004c0005t0016g0009a0004c0005t0016g0010 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.201+1169C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970018 | ||||||
chr16:83970050
|
C | CAAACCAT others(8): Show |
1 | a0002c0002t0008g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.201+1202_201+1216d others(17): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 83970050 | |||||
chr16:83970104
|
G | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.201+1255G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970104 | ||||||
chr16:83970132
|
T | C | 38 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(35): Show | 38 | HG01243.hp2 HG01255.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.201+1283T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970132 | ||||||
chr16:83970203
|
G | C | 1 | a0003c0008t0004g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.201+1354G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970203 | ||||||
chr16:83970277
|
C | G | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.201+1428C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970277 | ||||||
chr16:83970362
|
C | A | 1 | a0010c0034t0002g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.201+1513C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970362 | ||||||
chr16:83970441
|
A | G | 138 | a0001c0001t0001g0347a0001c0001t0005g0284a0001c0001t0005g0286others(135): Show | 138 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(135): Show |
intron_variant | MODIFIER | c.201+1592A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970441 | ||||||
chr16:83970456
|
A | C | 1 | a0003c0004t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.201+1607A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970456 | ||||||
chr16:83970491
|
G | T | 4 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.201+1642G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970491 | ||||||
chr16:83970516
|
G | T | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.202-1635G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970516 | ||||||
chr16:83970540
|
C | T | 11 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(8): Show | 11 | HG01255.hp1 HG01496.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-1611C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970540 | ||||||
chr16:83970550
|
G | A | 13 | a0002c0002t0047g0030a0002c0003t0003g0229a0002c0003t0004g0230others(10): Show | 13 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.202-1601G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970550 | ||||||
chr16:83970592
|
C | G | 3 | a0002c0003t0010g0221a0003c0004t0025g0222a0003c0004t0025g0223 | 3 | HG01167.hp1 HG01169.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.202-1559C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970592 | ||||||
chr16:83970677
|
T | G | 50 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0007g0211others(47): Show | 50 | HG01243.hp2 HG01255.hp1 HG01496.hp1 others(47): Show |
intron_variant | MODIFIER | c.202-1474T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970677 | ||||||
chr16:83970712
|
C | G | 1 | a0002c0002t0001g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.202-1439C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970712 | ||||||
chr16:83970736
|
T | A | 2 | a0004c0005t0016g0009a0004c0005t0016g0010 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.202-1415T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970736 | ||||||
chr16:83970891
|
G | A | 1 | a0003c0004t0040g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-1260G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970891 | ||||||
chr16:83970893
|
G | C | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0004c0036t0005g0214 | 3 | HG02723.hp2 HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.202-1258G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970893 | ||||||
chr16:83970969
|
C | T | 2 | a0003c0008t0004g0015a0003c0008t0004g0017 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.202-1182C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83970969 | ||||||
chr16:83971017
|
C | T | 3 | a0002c0003t0012g0325a0002c0003t0012g0326a0002c0003t0012g0327 | 3 | HG02818.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.202-1134C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971017 | ||||||
chr16:83971048
|
C | T | 7 | a0001c0001t0001g0347a0001c0001t0007g0322a0002c0002t0024g0323others(4): Show | 7 | HG01975.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.202-1103C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971048 | ||||||
chr16:83971093
|
CA | C | 95 | a0001c0001t0001g0206a0001c0001t0001g0347a0001c0001t0002g0346others(92): Show | 95 | HG01169.hp2 HG01255.hp1 HG01255.hp2 others(92): Show |
intron_variant | MODIFIER | c.202-1044delA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 83971093 | |||||
chr16:83971093
|
CAA | C | 8 | a0001c0006t0003g0336a0002c0002t0047g0030a0002c0003t0003g0296others(5): Show | 8 | HG01167.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.202-1045_202-1044d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 83971093 | |||||
chr16:83971217
|
C | G | 56 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0011g0200others(53): Show | 56 | HG01081.hp1 HG01168.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.202-934C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971217 | ||||||
chr16:83971252
|
C | G | 1 | a0005c0027t0045g0288 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.202-899C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971252 | ||||||
chr16:83971467
|
C | T | 1 | a0001c0006t0002g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.202-684C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971467 | ||||||
chr16:83971488
|
C | G | 1 | a0003c0004t0040g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-663C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971488 | ||||||
chr16:83971592
|
G | A | 1 | a0003c0028t0034g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.202-559G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971592 | ||||||
chr16:83971648
|
G | A | 57 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(54): Show | 57 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(54): Show |
intron_variant | MODIFIER | c.202-503G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971648 | ||||||
chr16:83971659
|
C | T | 3 | a0002c0002t0001g0197a0002c0002t0001g0198a0002c0002t0001g0199 | 3 | NA18986.hp2 NA19007.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.202-492C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971659 | ||||||
chr16:83971660
|
G | A | 3 | a0002c0011t0004g0291a0002c0011t0004g0292a0002c0011t0004g0293 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.202-491G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971660 | ||||||
chr16:83971700
|
G | A | 1 | a0001c0006t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.202-451G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971700 | ||||||
chr16:83971856
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.202-295C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971856 | ||||||
chr16:83971885
|
C | T | 32 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(29): Show | 32 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.202-266C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971885 | ||||||
chr16:83971909
|
A | C | 1 | a0002c0002t0001g0195 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.202-242A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971909 | ||||||
chr16:83971946
|
T | C | 48 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(45): Show | 48 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(45): Show |
intron_variant | MODIFIER | c.202-205T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971946 | ||||||
chr16:83971960
|
C | A | 1 | a0004c0005t0010g0237 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.202-191C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971960 | ||||||
chr16:83971967
|
C | T | 3 | a0003c0016t0020g0032a0008c0014t0003g0194a0008c0014t0038g0236 | 3 | HG02257.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.202-184C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971967 | ||||||
chr16:83971972
|
T | A | 3 | a0004c0018t0001g0040a0005c0009t0006g0038a0005c0009t0006g0039 | 3 | NA18944.hp2 NA18950.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.202-179T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971972 | ||||||
chr16:83971981
|
A | G | 3 | a0003c0008t0004g0015a0006c0012t0015g0013a0006c0012t0015g0014 | 3 | HG02145.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.202-170A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971981 | ||||||
chr16:83971984
|
T | A | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.202-167T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971984 | ||||||
chr16:83971991
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG00099.hp1 HG00642.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.202-160G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971991 | ||||||
chr16:83971994
|
T | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.202-157T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83971994 | ||||||
chr16:83972007
|
A | AG | 9 | a0001c0001t0002g0006a0001c0001t0002g0189a0001c0001t0002g0191others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.202-139dupG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 83972007 | |||||
chr16:83972067
|
A | T | 1 | a0003c0004t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.202-84A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83972067 | ||||||
chr16:83972082
|
C | T | 1 | a0003c0004t0040g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.202-69C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 1/12 | chr16 | 83972082 | ||||||
chr16:83972184
|
C | T | 37 | a0001c0001t0016g0258a0001c0006t0003g0336a0001c0006t0005g0256others(34): Show | 37 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.226+9C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972184 | ||||||
chr16:83972196
|
G | A | 61 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(58): Show | 61 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(58): Show |
intron_variant | MODIFIER | c.226+21G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972196 | ||||||
chr16:83972212
|
C | T | 5 | a0001c0001t0001g0184a0001c0001t0002g0182a0001c0001t0002g0183others(2): Show | 5 | HG00597.hp1 HG02071.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+37C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972212 | ||||||
chr16:83972311
|
C | G | 3 | a0001c0001t0016g0258a0001c0006t0005g0256a0003c0004t0004g0257 | 3 | HG02615.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.226+136C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972311 | ||||||
chr16:83972373
|
C | T | 1 | a0001c0006t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.226+198C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972373 | ||||||
chr16:83972526
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.226+351C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972526 | ||||||
chr16:83972530
|
G | T | 62 | a0001c0001t0016g0258a0001c0006t0003g0336a0001c0006t0005g0256others(59): Show | 62 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.226+355G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972530 | ||||||
chr16:83972591
|
A | G | 1 | a0003c0004t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226+416A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972591 | ||||||
chr16:83972678
|
G | A | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+503G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972678 | ||||||
chr16:83972698
|
C | G | 1 | a0002c0002t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.226+523C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972698 | ||||||
chr16:83972729
|
C | G | 37 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(34): Show | 37 | HG01255.hp2 HG01433.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.226+554C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972729 | ||||||
chr16:83972760
|
CTTG | C | 3 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297 | 3 | HG02647.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.226+590_226+592del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83972760 | |||||
chr16:83972799
|
C | G | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.226+624C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972799 | ||||||
chr16:83972820
|
C | G | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.226+645C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972820 | ||||||
chr16:83972824
|
CAGA | C | 4 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+652_226+654del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83972824 | |||||
chr16:83972864
|
C | A | 144 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(141): Show | 144 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(141): Show |
intron_variant | MODIFIER | c.226+689C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972864 | ||||||
chr16:83972943
|
C | T | 1 | a0002c0002t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.226+768C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972943 | ||||||
chr16:83972960
|
G | A | 33 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(30): Show | 33 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.226+785G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83972960 | ||||||
chr16:83973016
|
T | G | 4 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+841T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973016 | ||||||
chr16:83973075
|
A | G | 1 | a0002c0002t0003g0318 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.226+900A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973075 | ||||||
chr16:83973084
|
A | G | 1 | a0005c0027t0045g0288 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.226+909A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973084 | ||||||
chr16:83973095
|
G | A | 1 | a0002c0002t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.226+920G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973095 | ||||||
chr16:83973164
|
C | G | 140 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+989C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973164 | ||||||
chr16:83973221
|
C | T | 5 | a0002c0002t0003g0176a0002c0002t0003g0318a0002c0002t0019g0175others(2): Show | 5 | HG02451.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+1046C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973221 | ||||||
chr16:83973244
|
C | G | 140 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+1069C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973244 | ||||||
chr16:83973315
|
C | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1140C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973315 | ||||||
chr16:83973334
|
G | C | 25 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(22): Show | 25 | HG01256.hp2 HG01258.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+1159G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973334 | ||||||
chr16:83973368
|
G | A | 1 | a0004c0005t0043g0303 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226+1193G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973368 | ||||||
chr16:83973421
|
C | G | 17 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(14): Show | 17 | HG01884.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.226+1246C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973421 | ||||||
chr16:83973523
|
G | A | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.226+1348G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973523 | ||||||
chr16:83973626
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.226+1451G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973626 | ||||||
chr16:83973640
|
C | T | 1 | a0004c0005t0043g0303 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226+1465C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973640 | ||||||
chr16:83973717
|
C | T | 18 | a0001c0006t0005g0275a0001c0006t0005g0277a0002c0003t0010g0221others(15): Show | 18 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.226+1542C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973717 | ||||||
chr16:83973729
|
A | C | 1 | a0001c0001t0001g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.226+1554A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973729 | ||||||
chr16:83973818
|
C | G | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+1643C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973818 | ||||||
chr16:83973849
|
G | A | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226+1674G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973849 | ||||||
chr16:83973954
|
T | A | 53 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(50): Show | 53 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+1779T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973954 | ||||||
chr16:83973960
|
A | G | 151 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(148): Show | 151 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(148): Show |
intron_variant | MODIFIER | c.226+1785A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83973960 | ||||||
chr16:83974036
|
CCA | C | 52 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(49): Show | 52 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.226+1863_226+1864d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974036 | |||||
chr16:83974042
|
C | A | 5 | a0001c0001t0002g0346a0001c0001t0009g0343a0001c0001t0011g0342others(2): Show | 5 | HG02683.hp1 HG02698.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+1867C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974042 | ||||||
chr16:83974044
|
T | C | 52 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(49): Show | 52 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.226+1869T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974044 | ||||||
chr16:83974064
|
TCA | T | 3 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254 | 3 | HG01891.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.226+1890_226+1891d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974064 | ||||||
chr16:83974088
|
C | T | 2 | a0002c0002t0001g0170a0002c0002t0001g0171 | 2 | NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.226+1913C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974088 | ||||||
chr16:83974138
|
C | T | 1 | a0001c0006t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.226+1963C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974138 | ||||||
chr16:83974150
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.226+1975G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974150 | ||||||
chr16:83974177
|
G | A | 4 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2002G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974177 | ||||||
chr16:83974203
|
A | T | 3 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.226+2028A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974203 | ||||||
chr16:83974244
|
C | T | 53 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0002t0003g0253others(50): Show | 53 | HG01255.hp2 HG01433.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.226+2069C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974244 | ||||||
chr16:83974262
|
G | T | 1 | a0001c0007t0006g0169 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.226+2087G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974262 | ||||||
chr16:83974401
|
A | G | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226+2226A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974401 | ||||||
chr16:83974410
|
C | A | 136 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(133): Show | 136 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.226+2235C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974410 | ||||||
chr16:83974504
|
C | T | 1 | a0002c0003t0010g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.226+2329C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974504 | ||||||
chr16:83974512
|
G | C | 2 | a0002c0003t0003g0304a0002c0003t0003g0319 | 2 | NA19057.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.226+2337G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974512 | ||||||
chr16:83974553
|
T | A | 1 | a0004c0005t0016g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.226+2378T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974553 | ||||||
chr16:83974580
|
T | C | 4 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2405T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974580 | ||||||
chr16:83974584
|
G | A | 1 | a0003c0004t0030g0329 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.226+2409G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974584 | ||||||
chr16:83974618
|
C | T | 6 | a0002c0003t0004g0260a0002c0003t0004g0261a0002c0003t0012g0238others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+2443C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974618 | ||||||
chr16:83974645
|
C | G | 1 | a0011c0035t0001g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.226+2470C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974645 | ||||||
chr16:83974748
|
T | TTGGTGTG others(16): Show |
1 | a0004c0005t0043g0303 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.226+2583_226+2605d others(25): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974748 | |||||
chr16:83974762
|
G | T | 1 | a0002c0003t0007g0298 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.226+2587G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974762 | ||||||
chr16:83974769
|
G | C | 2 | a0003c0004t0023g0033a0003c0004t0023g0034 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.226+2594G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974769 | ||||||
chr16:83974773
|
G | T | 1 | a0002c0002t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.226+2598G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974773 | ||||||
chr16:83974790
|
G | C | 8 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+2615G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974790 | ||||||
chr16:83974858
|
G | A | 140 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0001t0016g0258others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.226+2683G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974858 | ||||||
chr16:83974875
|
T | C | 64 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(61): Show | 64 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(61): Show |
intron_variant | MODIFIER | c.226+2700T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974875 | ||||||
chr16:83974894
|
G | GCAGGTGT others(29): Show |
2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.226+2735_226+2736i others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974894 | |||||
chr16:83974911
|
C | T | 38 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(35): Show | 38 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.226+2736C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974911 | ||||||
chr16:83974920
|
G | A | 37 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(34): Show | 37 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.226+2745G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974920 | ||||||
chr16:83974920
|
G | GGGGATGG others(28): Show |
1 | a0004c0005t0005g0268 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.226+2767_226+2768i others(37): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974920 | |||||
chr16:83974920
|
G | GGGGATGG others(29): Show |
1 | a0002c0003t0010g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.226+2781_226+2816d others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974920 | |||||
chr16:83974920
|
GGGGATGG others(29): Show |
G | 9 | a0003c0004t0003g0035a0003c0004t0023g0033a0003c0004t0023g0034others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.226+2781_226+2816d others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974920 | |||||
chr16:83974930
|
A | ACAGGTGT others(29): Show |
36 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(33): Show | 36 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.226+2787_226+2788i others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974930 | |||||
chr16:83974951
|
G | GGTGCGGG others(45): Show |
4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2780_226+2781i others(54): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974951 | |||||
chr16:83974951
|
G | GGTGCGGG others(253): Show |
3 | a0003c0004t0039g0242a0004c0005t0005g0240a0004c0005t0005g0241 | 3 | HG01433.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.226+2780_226+2781i others(262): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974951 | |||||
chr16:83974963
|
G | A | 7 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(4): Show | 7 | HG01433.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+2788G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974963 | ||||||
chr16:83974966
|
A | G | 7 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(4): Show | 7 | HG01433.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+2791A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974966 | ||||||
chr16:83974991
|
C | CGGGGATG others(206): Show |
1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.226+2819_226+2820i others(215): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83974991 | |||||
chr16:83974992
|
G | A | 26 | a0001c0006t0005g0275a0001c0006t0005g0277a0002c0002t0003g0253others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.226+2817G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974992 | ||||||
chr16:83974995
|
A | G | 26 | a0001c0006t0005g0275a0001c0006t0005g0277a0002c0002t0003g0253others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.226+2820A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974995 | ||||||
chr16:83974999
|
T | A | 7 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(4): Show | 7 | HG01433.hp2 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+2824T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974999 | ||||||
chr16:83974999
|
T | G | 19 | a0001c0006t0005g0275a0001c0006t0005g0277a0002c0003t0003g0304others(16): Show | 19 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.226+2824T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83974999 | ||||||
chr16:83975003
|
C | CAGGTGTG others(137): Show |
17 | a0001c0006t0005g0275a0001c0006t0005g0277a0003c0004t0007g0276others(14): Show | 17 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.226+2828_226+2829i others(146): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975003 | ||||||
chr16:83975003
|
C | CAGGTGTG others(25): Show |
3 | a0003c0004t0039g0242a0004c0005t0005g0240a0004c0005t0005g0241 | 3 | HG01433.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.226+2828_226+2829i others(34): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975003 | ||||||
chr16:83975004
|
C | A | 25 | a0001c0006t0005g0275a0001c0006t0005g0277a0002c0002t0003g0253others(22): Show | 25 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+2829C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975004 | ||||||
chr16:83975004
|
C | CGGTGTGC others(137): Show |
1 | a0004c0005t0005g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.226+2841_226+2842i others(146): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975004
|
C | CGGTGTGC others(25): Show |
1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226+2868_226+2899d others(34): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975004
|
C | CGGTGTGC others(81): Show |
4 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0004t0033g0297others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2912_226+2999d others(90): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975004
|
C | CGGTGTGC others(113): Show |
4 | a0002c0003t0010g0221a0003c0004t0010g0234a0003c0004t0010g0235others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2868_226+2987d others(122): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975004
|
C | CGGTGTGC others(201): Show |
1 | a0001c0001t0052g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.226+3017_226+3018i others(210): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975004
|
C | CGGTGTGC others(101): Show |
1 | a0004c0005t0005g0268 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.226+2861_226+2862i others(110): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975004 | |||||
chr16:83975071
|
TGTGG | T | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2900_226+2903d others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975071 | |||||
chr16:83975090
|
A | G | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2915A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975090 | ||||||
chr16:83975091
|
C | CAGGTGTG others(25): Show |
4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2956_226+2987d others(34): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975091 | |||||
chr16:83975091
|
CAGGTGTG others(25): Show |
C | 1 | a0001c0006t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.226+2956_226+2987d others(34): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975091 | |||||
chr16:83975095
|
T | TGTGCAGG others(9): Show |
4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2929_226+2930i others(18): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975095 | |||||
chr16:83975122
|
G | C | 8 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+2947G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975122 | ||||||
chr16:83975159
|
TGTGG | T | 32 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(29): Show | 32 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.226+2988_226+2991d others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975159 | |||||
chr16:83975162
|
G | T | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2987G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975162 | ||||||
chr16:83975162
|
GGGTGCAG others(29): Show |
G | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.226+2993_226+3028d others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975162 | |||||
chr16:83975163
|
G | GGTGCAGG others(57): Show |
4 | a0003c0008t0004g0036a0003c0008t0004g0208a0003c0008t0004g0209others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2999_226+3000i others(66): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975163 | |||||
chr16:83975168
|
A | AGGGATGG others(29): Show |
6 | a0001c0001t0001g0164a0001c0001t0001g0174a0002c0002t0011g0163others(3): Show | 6 | HG03669.hp1 HG03688.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+3032_226+3067d others(38): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83975168 | |||||
chr16:83975168
|
A | G | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.226+2993A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975168 | ||||||
chr16:83975175
|
G | A | 36 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(33): Show | 36 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.226+3000G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975175 | ||||||
chr16:83975178
|
A | G | 36 | a0001c0001t0016g0258a0001c0006t0005g0256a0002c0003t0003g0229others(33): Show | 36 | HG01255.hp2 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.226+3003A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975178 | ||||||
chr16:83975300
|
A | G | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.226+3125A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975300 | ||||||
chr16:83975363
|
C | G | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.227-3081C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975363 | ||||||
chr16:83975404
|
C | G | 8 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-3040C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975404 | ||||||
chr16:83975441
|
C | G | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.227-3003C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975441 | ||||||
chr16:83975445
|
C | G | 3 | a0002c0002t0001g0160a0002c0002t0001g0161a0002c0002t0001g0162 | 3 | HG02523.hp1 NA18983.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.227-2999C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975445 | ||||||
chr16:83975507
|
T | C | 1 | a0003c0008t0004g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.227-2937T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975507 | ||||||
chr16:83975515
|
C | T | 54 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(51): Show | 54 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(51): Show |
intron_variant | MODIFIER | c.227-2929C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975515 | ||||||
chr16:83975520
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.227-2924C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975520 | ||||||
chr16:83975541
|
A | G | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-2903A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975541 | ||||||
chr16:83975621
|
G | A | 1 | a0002c0002t0001g0197 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.227-2823G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975621 | ||||||
chr16:83975627
|
C | G | 3 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.227-2817C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975627 | ||||||
chr16:83975704
|
G | T | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.227-2740G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975704 | ||||||
chr16:83975724
|
C | T | 4 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(1): Show | 4 | HG01891.hp1 HG03453.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-2720C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975724 | ||||||
chr16:83975734
|
A | T | 56 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(53): Show | 56 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(53): Show |
intron_variant | MODIFIER | c.227-2710A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975734 | ||||||
chr16:83975797
|
T | C | 142 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(139): Show | 142 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(139): Show |
intron_variant | MODIFIER | c.227-2647T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975797 | ||||||
chr16:83975843
|
T | C | 10 | a0003c0004t0003g0035a0003c0004t0023g0033a0003c0004t0023g0034others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.227-2601T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975843 | ||||||
chr16:83975847
|
A | G | 55 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(52): Show | 55 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(52): Show |
intron_variant | MODIFIER | c.227-2597A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975847 | ||||||
chr16:83975848
|
A | G | 3 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254 | 3 | HG01891.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.227-2596A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975848 | ||||||
chr16:83975883
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.227-2561T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975883 | ||||||
chr16:83975892
|
G | A | 8 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-2552G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975892 | ||||||
chr16:83975902
|
G | C | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-2542G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83975902 | ||||||
chr16:83976026
|
C | G | 1 | a0001c0006t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.227-2418C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976026 | ||||||
chr16:83976103
|
C | T | 8 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(5): Show | 8 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-2341C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976103 | ||||||
chr16:83976143
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.227-2301G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976143 | ||||||
chr16:83976211
|
C | G | 1 | a0007c0017t0014g0287 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.227-2233C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976211 | ||||||
chr16:83976236
|
G | C | 143 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(140): Show | 143 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(140): Show |
intron_variant | MODIFIER | c.227-2208G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976236 | ||||||
chr16:83976299
|
G | C | 1 | a0003c0028t0034g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.227-2145G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976299 | ||||||
chr16:83976323
|
T | G | 3 | a0002c0011t0004g0291a0002c0011t0004g0292a0002c0011t0004g0293 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-2121T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976323 | ||||||
chr16:83976444
|
C | A | 1 | a0002c0003t0010g0330 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.227-2000C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976444 | ||||||
chr16:83976495
|
C | G | 3 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.227-1949C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976495 | ||||||
chr16:83976539
|
A | C | 142 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(139): Show | 142 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(139): Show |
intron_variant | MODIFIER | c.227-1905A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976539 | ||||||
chr16:83976571
|
C | T | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-1873C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976571 | ||||||
chr16:83976666
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1778T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976666 | ||||||
chr16:83976667
|
T | C | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1777T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976667 | ||||||
chr16:83976668
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1776C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976668 | ||||||
chr16:83976670
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1774T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976670 | ||||||
chr16:83976677
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.227-1767G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976677 | ||||||
chr16:83976681
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1763C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976681 | ||||||
chr16:83976686
|
A | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1758A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976686 | ||||||
chr16:83976688
|
A | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1756A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976688 | ||||||
chr16:83976699
|
G | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0051 | 2 | HG02056.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.227-1745G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976699 | ||||||
chr16:83976700
|
A | ATGT | 142 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(139): Show | 142 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(139): Show |
intron_variant | MODIFIER | c.227-1742_227-1741i others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 83976700 | |||||
chr16:83976734
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1710C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976734 | ||||||
chr16:83976736
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1708T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976736 | ||||||
chr16:83976740
|
C | G | 1 | a0001c0001t0002g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.227-1704C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976740 | ||||||
chr16:83976741
|
A | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1703A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976741 | ||||||
chr16:83976742
|
C | G | 137 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(134): Show | 137 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.227-1702C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976742 | ||||||
chr16:83976742
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1702C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976742 | ||||||
chr16:83976744
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1700C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976744 | ||||||
chr16:83976748
|
C | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1696C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976748 | ||||||
chr16:83976749
|
A | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1695A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976749 | ||||||
chr16:83976751
|
A | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1693A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976751 | ||||||
chr16:83976752
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1692T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976752 | ||||||
chr16:83976754
|
C | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1690C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976754 | ||||||
chr16:83976756
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1688T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976756 | ||||||
chr16:83976757
|
T | A | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1687T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976757 | ||||||
chr16:83976759
|
C | A | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1685C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976759 | ||||||
chr16:83976759
|
C | G | 2 | a0003c0016t0020g0216a0004c0036t0005g0214 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.227-1685C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976759 | ||||||
chr16:83976760
|
C | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1684C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976760 | ||||||
chr16:83976761
|
G | T | 2 | a0003c0016t0020g0216a0004c0036t0005g0214 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.227-1683G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976761 | ||||||
chr16:83976764
|
C | A | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-1680C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976764 | ||||||
chr16:83976813
|
A | C | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1631A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976813 | ||||||
chr16:83976825
|
A | C | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1619A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976825 | ||||||
chr16:83976904
|
A | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1540A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976904 | ||||||
chr16:83976905
|
A | C | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1539A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976905 | ||||||
chr16:83976907
|
C | T | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-1537C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976907 | ||||||
chr16:83976915
|
C | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1529C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976915 | ||||||
chr16:83976917
|
T | C | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1527T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976917 | ||||||
chr16:83976920
|
A | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1524A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976920 | ||||||
chr16:83976925
|
T | G | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1519T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976925 | ||||||
chr16:83976947
|
C | T | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-1497C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976947 | ||||||
chr16:83976955
|
G | A | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-1489G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83976955 | ||||||
chr16:83977012
|
A | G | 142 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(139): Show | 142 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(139): Show |
intron_variant | MODIFIER | c.227-1432A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977012 | ||||||
chr16:83977081
|
C | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.227-1363C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977081 | ||||||
chr16:83977096
|
A | T | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-1348A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977096 | ||||||
chr16:83977128
|
TGGACTCT others(13): Show |
T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1315_227-1296d others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977128 | ||||||
chr16:83977152
|
A | T | 1 | a0002c0003t0012g0325 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.227-1292A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977152 | ||||||
chr16:83977238
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.227-1206C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977238 | ||||||
chr16:83977315
|
C | T | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.227-1129C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977315 | ||||||
chr16:83977324
|
A | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.227-1120A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977324 | ||||||
chr16:83977325
|
G | T | 6 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316others(3): Show | 6 | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-1119G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977325 | ||||||
chr16:83977328
|
G | A | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-1116G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977328 | ||||||
chr16:83977328
|
G | T | 135 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(132): Show | 135 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(132): Show |
intron_variant | MODIFIER | c.227-1116G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977328 | ||||||
chr16:83977345
|
G | A | 54 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(51): Show | 54 | HG01255.hp1 HG01256.hp2 HG01258.hp2 others(51): Show |
intron_variant | MODIFIER | c.227-1099G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977345 | ||||||
chr16:83977367
|
C | G | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-1077C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977367 | ||||||
chr16:83977403
|
G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.227-1041G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977403 | ||||||
chr16:83977432
|
C | T | 1 | a0004c0005t0005g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.227-1012C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977432 | ||||||
chr16:83977439
|
C | T | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-1005C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977439 | ||||||
chr16:83977484
|
G | A | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-960G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977484 | ||||||
chr16:83977504
|
C | T | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-940C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977504 | ||||||
chr16:83977515
|
G | C | 25 | a0001c0006t0005g0256a0002c0026t0032g0012a0003c0004t0003g0243others(22): Show | 25 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.227-929G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977515 | ||||||
chr16:83977532
|
C | T | 132 | a0001c0001t0001g0347a0001c0001t0007g0322a0001c0006t0002g0022others(129): Show | 132 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(129): Show |
intron_variant | MODIFIER | c.227-912C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977532 | ||||||
chr16:83977593
|
A | G | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-851A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977593 | ||||||
chr16:83977604
|
C | T | 4 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009others(1): Show | 4 | HG02602.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-840C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977604 | ||||||
chr16:83977651
|
T | C | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.227-793T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977651 | ||||||
chr16:83977720
|
G | A | 2 | a0001c0001t0014g0300a0001c0001t0014g0301 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.227-724G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977720 | ||||||
chr16:83977802
|
A | G | 1 | a0003c0004t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227-642A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977802 | ||||||
chr16:83977840
|
A | G | 1 | a0002c0002t0008g0341 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.227-604A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977840 | ||||||
chr16:83977864
|
G | A | 1 | a0003c0004t0003g0243 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.227-580G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977864 | ||||||
chr16:83977889
|
G | C | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-555G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977889 | ||||||
chr16:83977925
|
G | C | 1 | a0003c0004t0021g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.227-519G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83977925 | ||||||
chr16:83978098
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0174a0002c0002t0011g0163others(1): Show | 4 | HG03669.hp1 HG03688.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-346G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83978098 | ||||||
chr16:83978313
|
G | A | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-131G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83978313 | ||||||
chr16:83978319
|
A | G | 1 | a0002c0003t0010g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.227-125A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83978319 | ||||||
chr16:83978374
|
G | A | 139 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(136): Show | 139 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-70G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83978374 | ||||||
chr16:83978425
|
T | C | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227-19T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 2/12 | chr16 | 83978425 | ||||||
chr16:83978610
|
C | G | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.335+58C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978610 | ||||||
chr16:83978610
|
C | T | 1 | a0004c0005t0007g0339 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.335+58C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978610 | ||||||
chr16:83978627
|
G | A | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.335+75G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978627 | ||||||
chr16:83978745
|
A | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+193A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978745 | ||||||
chr16:83978748
|
A | G | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.335+196A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978748 | ||||||
chr16:83978858
|
T | C | 3 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0008t0004g0210 | 3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.335+306T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978858 | ||||||
chr16:83978869
|
G | T | 1 | a0003c0008t0004g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.335+317G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978869 | ||||||
chr16:83978884
|
T | G | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.335+332T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978884 | ||||||
chr16:83978895
|
C | G | 3 | a0003c0015t0018g0203a0003c0015t0018g0204a0003c0015t0018g0205 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.335+343C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978895 | ||||||
chr16:83978944
|
G | C | 136 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(133): Show | 136 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.335+392G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978944 | ||||||
chr16:83978994
|
A | C | 4 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009others(1): Show | 4 | HG02602.hp2 HG02630.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.335+442A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83978994 | ||||||
chr16:83979000
|
C | T | 1 | a0002c0002t0001g0046 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.335+448C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979000 | ||||||
chr16:83979008
|
A | G | 2 | a0002c0002t0008g0031a0002c0003t0004g0267 | 2 | HG03017.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.335+456A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979008 | ||||||
chr16:83979080
|
C | T | 3 | a0004c0013t0017g0217a0004c0013t0017g0218a0004c0013t0017g0219 | 3 | HG03209.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.335+528C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979080 | ||||||
chr16:83979120
|
T | G | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+568T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979120 | ||||||
chr16:83979142
|
C | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335+590C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979142 | ||||||
chr16:83979231
|
G | A | 3 | a0003c0004t0039g0242a0004c0005t0005g0240a0004c0005t0005g0241 | 3 | HG01433.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.335+679G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979231 | ||||||
chr16:83979274
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.335+722G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979274 | ||||||
chr16:83979297
|
G | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.335+745G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979297 | ||||||
chr16:83979320
|
G | C | 1 | a0001c0001t0001g0054 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.335+768G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979320 | ||||||
chr16:83979362
|
C | G | 135 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(132): Show | 135 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(132): Show |
intron_variant | MODIFIER | c.335+810C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979362 | ||||||
chr16:83979380
|
C | T | 3 | a0003c0004t0007g0282a0004c0005t0005g0278a0004c0005t0005g0283 | 3 | NA18971.hp2 NA19074.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.335+828C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979380 | ||||||
chr16:83979383
|
G | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+831G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979383 | ||||||
chr16:83979411
|
T | C | 138 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(135): Show | 138 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.335+859T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979411 | ||||||
chr16:83979468
|
T | G | 1 | a0002c0002t0019g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.335+916T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979468 | ||||||
chr16:83979489
|
C | T | 14 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(11): Show | 14 | HG01255.hp1 HG01496.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.335+937C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979489 | ||||||
chr16:83979531
|
C | G | 137 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(134): Show | 137 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.335+979C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979531 | ||||||
chr16:83979536
|
C | T | 3 | a0002c0020t0003g0228a0003c0004t0040g0018a0004c0005t0016g0009 | 3 | HG02602.hp2 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.335+984C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979536 | ||||||
chr16:83979537
|
T | G | 137 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(134): Show | 137 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.335+985T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979537 | ||||||
chr16:83979553
|
G | C | 137 | a0001c0006t0002g0022a0001c0006t0002g0023a0001c0006t0002g0024others(134): Show | 137 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.335+1001G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979553 | ||||||
chr16:83979651
|
A | C | 7 | a0001c0006t0005g0277a0002c0003t0003g0229a0003c0008t0004g0036others(4): Show | 7 | HG00738.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.335+1099A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979651 | ||||||
chr16:83979656
|
C | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01109.hp2 HG01175.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.335+1104C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979656 | ||||||
chr16:83979733
|
T | C | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.336-1106T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979733 | ||||||
chr16:83979744
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.336-1095G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979744 | ||||||
chr16:83979756
|
G | C | 1 | a0001c0001t0001g0206 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.336-1083G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979756 | ||||||
chr16:83979834
|
C | G | 11 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0007t0001g0141others(8): Show | 11 | HG00597.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.336-1005C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979834 | ||||||
chr16:83979877
|
A | G | 1 | a0002c0002t0007g0299 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.336-962A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83979877 | ||||||
chr16:83980073
|
G | A | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.336-766G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980073 | ||||||
chr16:83980096
|
A | C | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.336-743A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980096 | ||||||
chr16:83980206
|
A | G | 1 | a0003c0004t0003g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.336-633A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980206 | ||||||
chr16:83980241
|
A | G | 3 | a0002c0003t0003g0296a0003c0004t0022g0295a0003c0008t0004g0210 | 3 | HG02572.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.336-598A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980241 | ||||||
chr16:83980273
|
T | G | 140 | a0001c0001t0002g0056a0001c0001t0016g0258a0001c0006t0002g0022others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.336-566T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980273 | ||||||
chr16:83980282
|
G | T | 14 | a0001c0006t0005g0275a0003c0004t0007g0276a0003c0004t0007g0282others(11): Show | 14 | HG00642.hp2 HG02132.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.336-557G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980282 | ||||||
chr16:83980332
|
G | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(3): Show | 6 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.336-507G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980332 | ||||||
chr16:83980369
|
T | C | 140 | a0001c0001t0002g0056a0001c0001t0016g0258a0001c0006t0002g0022others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.336-470T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980369 | ||||||
chr16:83980462
|
A | C | 139 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(136): Show | 139 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(136): Show |
intron_variant | MODIFIER | c.336-377A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980462 | ||||||
chr16:83980468
|
G | C | 136 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(133): Show | 136 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.336-371G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980468 | ||||||
chr16:83980469
|
G | A | 20 | a0001c0006t0005g0275a0003c0004t0007g0276a0003c0004t0007g0282others(17): Show | 20 | HG00642.hp2 HG00741.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.336-370G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980469 | ||||||
chr16:83980508
|
G | A | 1 | a0001c0001t0011g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.336-331G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980508 | ||||||
chr16:83980699
|
C | G | 1 | a0006c0012t0003g0312 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.336-140C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980699 | ||||||
chr16:83980754
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.336-85A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980754 | ||||||
chr16:83980765
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.336-74G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 3/12 | chr16 | 83980765 | ||||||
chr16:83980877
|
C | G | 138 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(135): Show | 138 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.361+13C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 4/12 | chr16 | 83980877 | ||||||
chr16:83980958
|
G | A | 135 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(132): Show | 135 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(132): Show |
intron_variant | MODIFIER | c.362-72G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 4/12 | chr16 | 83980958 | ||||||
chr16:83980967
|
G | A | 1 | a0004c0005t0016g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.362-63G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 4/12 | chr16 | 83980967 | ||||||
chr16:83981020
|
C | T | 3 | a0003c0015t0018g0203a0003c0015t0018g0204a0003c0015t0018g0205 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.362-10C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 4/12 | chr16 | 83981020 | ||||||
chr16:83981026
|
C | T | 12 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.362-4C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 4/12 | chr16 | 83981026 | ||||||
chr16:83981143
|
T | G | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459+16T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981143 | ||||||
chr16:83981150
|
C | T | 1 | a0003c0004t0007g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.459+23C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981150 | ||||||
chr16:83981154
|
G | GTCCAGGG others(1): Show |
138 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(135): Show | 138 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.459+33_459+40dupGG others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83981154 | |||||
chr16:83981173
|
C | A | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+46C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981173 | ||||||
chr16:83981173
|
C | T | 3 | a0003c0015t0018g0203a0003c0015t0018g0204a0003c0015t0018g0205 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.459+46C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981173 | ||||||
chr16:83981235
|
A | G | 4 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(1): Show | 4 | HG01884.hp2 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+108A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981235 | ||||||
chr16:83981236
|
T | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459+109T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981236 | ||||||
chr16:83981330
|
A | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+203A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981330 | ||||||
chr16:83981409
|
AG | A | 39 | a0002c0003t0010g0221a0002c0003t0012g0238a0002c0003t0012g0325others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.459+286delG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83981409 | |||||
chr16:83981429
|
C | T | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+302C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981429 | ||||||
chr16:83981435
|
C | G | 1 | a0002c0002t0009g0139 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.459+308C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981435 | ||||||
chr16:83981524
|
C | G | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+397C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981524 | ||||||
chr16:83981567
|
C | A | 2 | a0002c0002t0001g0057a0002c0002t0007g0299 | 2 | NA18980.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.459+440C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981567 | ||||||
chr16:83981708
|
T | G | 138 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(135): Show | 138 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.459+581T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981708 | ||||||
chr16:83981803
|
G | C | 2 | a0003c0004t0040g0018a0004c0005t0016g0009 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+676G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981803 | ||||||
chr16:83981851
|
C | T | 1 | a0004c0005t0007g0339 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.459+724C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981851 | ||||||
chr16:83981861
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459+734C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981861 | ||||||
chr16:83981884
|
T | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459+757T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981884 | ||||||
chr16:83981932
|
C | T | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.459+805C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981932 | ||||||
chr16:83981935
|
G | A | 125 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(122): Show | 125 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(122): Show |
intron_variant | MODIFIER | c.459+808G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981935 | ||||||
chr16:83981949
|
A | C | 2 | a0003c0004t0004g0257a0004c0005t0005g0251 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.459+822A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981949 | ||||||
chr16:83981978
|
G | A | 1 | a0001c0001t0002g0178 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.459+851G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981978 | ||||||
chr16:83981992
|
C | G | 2 | a0003c0004t0004g0257a0004c0005t0005g0251 | 2 | HG02109.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.459+865C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83981992 | ||||||
chr16:83982111
|
T | A | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+984T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982111 | ||||||
chr16:83982141
|
A | C | 3 | a0001c0006t0003g0336a0001c0006t0005g0256a0002c0003t0031g0310 | 3 | HG02055.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.459+1014A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982141 | ||||||
chr16:83982158
|
C | T | 1 | a0001c0007t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.459+1031C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982158 | ||||||
chr16:83982207
|
CAGTT | C | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1084_459+1087d others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83982207 | |||||
chr16:83982209
|
G | C | 125 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(122): Show | 125 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(122): Show |
intron_variant | MODIFIER | c.459+1082G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982209 | ||||||
chr16:83982218
|
C | T | 2 | a0002c0002t0008g0341a0002c0002t0013g0340 | 2 | HG00423.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.459+1091C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982218 | ||||||
chr16:83982252
|
A | G | 1 | a0008c0014t0038g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.459+1125A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982252 | ||||||
chr16:83982258
|
C | A | 128 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(125): Show | 128 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(125): Show |
intron_variant | MODIFIER | c.459+1131C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982258 | ||||||
chr16:83982292
|
C | G | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1165C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982292 | ||||||
chr16:83982459
|
G | A | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+1332G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982459 | ||||||
chr16:83982535
|
C | T | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+1408C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982535 | ||||||
chr16:83982538
|
T | C | 1 | a0001c0001t0011g0200 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.459+1411T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982538 | ||||||
chr16:83982539
|
G | A | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+1412G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982539 | ||||||
chr16:83982578
|
T | C | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1451T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982578 | ||||||
chr16:83982656
|
T | C | 7 | a0003c0004t0023g0033a0003c0004t0023g0034a0004c0013t0017g0217others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+1529T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982656 | ||||||
chr16:83982701
|
A | C | 86 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(83): Show | 86 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.459+1574A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982701 | ||||||
chr16:83982711
|
A | G | 1 | a0001c0001t0009g0137 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.459+1584A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982711 | ||||||
chr16:83982718
|
C | T | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459+1591C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982718 | ||||||
chr16:83982722
|
T | A | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1595T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982722 | ||||||
chr16:83982740
|
T | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.459+1613T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982740 | ||||||
chr16:83982758
|
T | C | 126 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(123): Show | 126 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(123): Show |
intron_variant | MODIFIER | c.459+1631T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982758 | ||||||
chr16:83982763
|
G | A | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1636G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982763 | ||||||
chr16:83982807
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.459+1680G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982807 | ||||||
chr16:83982861
|
C | G | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1734C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982861 | ||||||
chr16:83982878
|
T | G | 131 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(128): Show | 131 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(128): Show |
intron_variant | MODIFIER | c.459+1751T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982878 | ||||||
chr16:83982939
|
C | G | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+1812C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982939 | ||||||
chr16:83982951
|
C | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0162 | 2 | NA18983.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.459+1824C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982951 | ||||||
chr16:83982956
|
C | T | 1 | a0002c0002t0008g0135 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.459+1829C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83982956 | ||||||
chr16:83983022
|
C | T | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.459+1895C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983022 | ||||||
chr16:83983042
|
T | C | 1 | a0002c0002t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.459+1915T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983042 | ||||||
chr16:83983060
|
G | T | 3 | a0003c0004t0040g0018a0003c0016t0020g0216a0004c0005t0016g0009 | 3 | HG03486.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+1933G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983060 | ||||||
chr16:83983092
|
G | C | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+1965G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983092 | ||||||
chr16:83983100
|
T | C | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+1973T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983100 | ||||||
chr16:83983168
|
T | A | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.459+2041T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983168 | ||||||
chr16:83983189
|
G | C | 130 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(127): Show | 130 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+2062G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983189 | ||||||
chr16:83983220
|
G | A | 33 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(30): Show | 33 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+2093G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983220 | ||||||
chr16:83983257
|
T | C | 7 | a0002c0020t0003g0228a0003c0004t0025g0222a0003c0004t0025g0223others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+2130T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983257 | ||||||
chr16:83983371
|
G | A | 6 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+2244G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983371 | ||||||
chr16:83983373
|
C | T | 86 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(83): Show | 86 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.459+2246C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983373 | ||||||
chr16:83983385
|
C | T | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459+2258C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983385 | ||||||
chr16:83983453
|
A | G | 1 | a0004c0005t0016g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459+2326A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983453 | ||||||
chr16:83983484
|
T | A | 1 | a0001c0001t0009g0343 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.459+2357T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983484 | ||||||
chr16:83983514
|
C | A | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+2387C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983514 | ||||||
chr16:83983586
|
A | G | 1 | a0001c0006t0005g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+2459A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983586 | ||||||
chr16:83983616
|
G | T | 2 | a0002c0003t0004g0337a0003c0004t0030g0329 | 2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.459+2489G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983616 | ||||||
chr16:83983684
|
G | T | 12 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(9): Show | 12 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+2557G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983684 | ||||||
chr16:83983726
|
C | T | 1 | a0001c0001t0029g0134 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.459+2599C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983726 | ||||||
chr16:83983887
|
T | A | 1 | a0001c0001t0001g0060 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.459+2760T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983887 | ||||||
chr16:83983927
|
T | G | 1 | a0008c0014t0003g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.459+2800T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983927 | ||||||
chr16:83983979
|
C | CAT | 86 | a0001c0001t0001g0041a0001c0006t0002g0158a0001c0006t0003g0336others(83): Show | 86 | HG01255.hp1 HG01255.hp2 HG01256.hp1 others(83): Show |
intron_variant | MODIFIER | c.459+2863_459+2864d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983979 | |||||
chr16:83983979
|
C | CATAT | 11 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220others(8): Show | 11 | HG01433.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.459+2861_459+2864d others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983979 | |||||
chr16:83983980
|
A | G | 34 | a0001c0001t0002g0006a0001c0001t0002g0131a0001c0001t0002g0132others(31): Show | 34 | HG00558.hp2 HG00741.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.459+2853A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83983980 | ||||||
chr16:83983996
|
G | GT | 29 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(26): Show | 30 | HG00140.hp1 HG00609.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+2888dupT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983996 | |||||
chr16:83983996
|
GT | G | 26 | a0001c0001t0001g0061a0001c0001t0002g0131a0001c0001t0002g0132others(23): Show | 26 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.459+2888delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983996 | |||||
chr16:83983996
|
GTT | G | 93 | a0001c0001t0001g0041a0001c0001t0002g0006a0001c0001t0002g0192others(90): Show | 93 | HG00558.hp2 HG00741.hp2 HG01175.hp1 others(90): Show |
intron_variant | MODIFIER | c.459+2887_459+2888d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983996 | |||||
chr16:83983996
|
GTTT | G | 8 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(5): Show | 8 | HG01167.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+2886_459+2888d others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83983996 | |||||
chr16:83984019
|
G | A | 2 | a0003c0004t0022g0295a0003c0008t0004g0210 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.459+2892G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984019 | ||||||
chr16:83984035
|
A | G | 1 | a0002c0003t0007g0308 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.459+2908A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984035 | ||||||
chr16:83984036
|
T | C | 1 | a0002c0003t0007g0308 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.459+2909T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984036 | ||||||
chr16:83984041
|
G | C | 3 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313 | 3 | HG01167.hp1 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.459+2914G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984041 | ||||||
chr16:83984082
|
G | A | 1 | a0002c0002t0007g0299 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.459+2955G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984082 | ||||||
chr16:83984084
|
C | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+2957C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984084 | ||||||
chr16:83984097
|
G | A | 2 | a0001c0007t0001g0156a0002c0003t0044g0309 | 2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.459+2970G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984097 | ||||||
chr16:83984120
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+2993C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984120 | ||||||
chr16:83984145
|
G | A | 1 | a0004c0005t0016g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.459+3018G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984145 | ||||||
chr16:83984147
|
T | C | 2 | a0008c0014t0003g0194a0008c0014t0038g0236 | 2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.459+3020T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984147 | ||||||
chr16:83984241
|
C | T | 29 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(26): Show | 29 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+3114C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984241 | ||||||
chr16:83984284
|
C | T | 2 | a0003c0004t0022g0295a0003c0008t0004g0210 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.459+3157C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984284 | ||||||
chr16:83984291
|
G | A | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.459+3164G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984291 | ||||||
chr16:83984291
|
G | T | 2 | a0002c0002t0008g0016a0002c0002t0008g0135 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.459+3164G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984291 | ||||||
chr16:83984292
|
G | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+3165G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984292 | ||||||
chr16:83984326
|
A | G | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.459+3199A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984326 | ||||||
chr16:83984329
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+3202C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984329 | ||||||
chr16:83984330
|
G | T | 3 | a0003c0004t0039g0242a0004c0005t0005g0240a0004c0005t0005g0241 | 3 | HG01433.hp2 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.459+3203G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984330 | ||||||
chr16:83984400
|
C | T | 13 | a0001c0006t0002g0158a0001c0007t0001g0156a0002c0003t0003g0007others(10): Show | 13 | HG02027.hp1 NA18747.hp1 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+3273C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984400 | ||||||
chr16:83984401
|
G | A | 31 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(28): Show | 31 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+3274G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984401 | ||||||
chr16:83984444
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.459+3317C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984444 | ||||||
chr16:83984450
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+3323C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984450 | ||||||
chr16:83984461
|
G | A | 12 | a0001c0001t0016g0258a0002c0002t0003g0253a0002c0002t0003g0255others(9): Show | 12 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+3334G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984461 | ||||||
chr16:83984488
|
C | T | 3 | a0003c0004t0007g0282a0004c0005t0005g0278a0004c0005t0005g0283 | 3 | NA18971.hp2 NA19074.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.459+3361C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984488 | ||||||
chr16:83984493
|
C | T | 1 | a0002c0003t0010g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+3366C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984493 | ||||||
chr16:83984617
|
C | T | 54 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(51): Show | 54 | HG01255.hp1 HG01496.hp1 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.459+3490C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984617 | ||||||
chr16:83984663
|
C | T | 1 | a0003c0004t0003g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.459+3536C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984663 | ||||||
chr16:83984689
|
C | T | 1 | a0001c0006t0002g0026 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.459+3562C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984689 | ||||||
chr16:83984774
|
G | T | 8 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+3647G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984774 | ||||||
chr16:83984986
|
G | C | 131 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(128): Show | 131 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(128): Show |
intron_variant | MODIFIER | c.459+3859G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83984986 | ||||||
chr16:83985079
|
G | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.459+3952G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985079 | ||||||
chr16:83985100
|
G | A | 65 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(62): Show | 65 | HG01255.hp1 HG01433.hp1 HG01496.hp1 others(62): Show |
intron_variant | MODIFIER | c.459+3973G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985100 | ||||||
chr16:83985248
|
G | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+4121G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985248 | ||||||
chr16:83985313
|
C | CA | 39 | a0001c0001t0001g0021a0001c0001t0001g0060a0001c0001t0001g0075others(36): Show | 39 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.459+4219dupA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAA | 26 | a0001c0001t0001g0001a0001c0001t0001g0181a0001c0001t0001g0184others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.459+4218_459+4219d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAA | 8 | a0001c0001t0001g0063a0001c0007t0006g0066a0002c0002t0001g0065others(5): Show | 8 | HG02027.hp2 HG03453.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+4217_459+4219d others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(7): Show |
1 | a0004c0005t0005g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.459+4206_459+4219d others(16): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(11): Show |
4 | a0003c0004t0007g0282a0004c0005t0005g0263a0004c0005t0005g0283others(1): Show | 4 | HG03017.hp1 NA18977.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4202_459+4219d others(20): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(12): Show |
2 | a0003c0004t0007g0276a0004c0005t0005g0272 | 2 | HG02132.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.459+4201_459+4219d others(21): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(13): Show |
4 | a0003c0004t0003g0035a0004c0005t0005g0270a0004c0005t0005g0271others(1): Show | 4 | HG01243.hp2 NA18953.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+4200_459+4219d others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(14): Show |
1 | a0001c0006t0005g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.459+4199_459+4219d others(23): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(15): Show |
2 | a0004c0005t0005g0241a0004c0005t0005g0269 | 2 | HG00741.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.459+4198_459+4219d others(24): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(16): Show |
1 | a0004c0005t0005g0240 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.459+4197_459+4219d others(25): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
C | CAAAAAAA others(17): Show |
1 | a0001c0006t0005g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.459+4196_459+4219d others(26): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CA | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0043others(67): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.459+4219delA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0121a0003c0004t0025g0222a0003c0004t0025g0223others(2): Show | 5 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+4210_459+4219d others(12): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0006t0005g0256a0002c0002t0003g0253a0002c0003t0003g0319others(2): Show | 5 | HG02055.hp2 HG03516.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+4208_459+4219d others(14): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(6): Show |
C | 49 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(46): Show | 49 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(46): Show |
intron_variant | MODIFIER | c.459+4207_459+4219d others(15): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(7): Show |
C | 4 | a0002c0002t0019g0175a0002c0011t0004g0292a0002c0026t0032g0012others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4206_459+4219d others(16): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(8): Show |
C | 47 | a0002c0003t0003g0229a0002c0003t0004g0230a0002c0003t0004g0232others(44): Show | 47 | HG01255.hp2 HG01433.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.459+4205_459+4219d others(17): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985313
|
CAAAAAAA others(9): Show |
C | 1 | a0003c0004t0039g0242 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+4204_459+4219d others(18): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985313 | |||||
chr16:83985361
|
G | T | 1 | a0004c0005t0005g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.459+4234G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985361 | ||||||
chr16:83985362
|
C | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+4235C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985362 | ||||||
chr16:83985377
|
G | C | 32 | a0001c0006t0005g0275a0001c0006t0005g0277a0003c0004t0003g0035others(29): Show | 32 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.459+4250G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985377 | ||||||
chr16:83985393
|
G | C | 4 | a0001c0001t0001g0107a0001c0001t0005g0286a0001c0001t0009g0137others(1): Show | 4 | HG00140.hp1 HG01515.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+4266G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985393 | ||||||
chr16:83985401
|
G | A | 3 | a0001c0006t0007g0211a0001c0006t0007g0212a0001c0006t0007g0213 | 3 | HG02135.hp1 NA18747.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.459+4274G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985401 | ||||||
chr16:83985408
|
A | G | 140 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(137): Show | 140 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(137): Show |
intron_variant | MODIFIER | c.459+4281A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985408 | ||||||
chr16:83985469
|
C | T | 1 | a0004c0005t0005g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+4342C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985469 | ||||||
chr16:83985546
|
T | C | 105 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(102): Show | 105 | HG01255.hp1 HG01255.hp2 HG01257.hp2 others(102): Show |
intron_variant | MODIFIER | c.459+4419T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985546 | ||||||
chr16:83985635
|
G | GA | 12 | a0001c0001t0052g0166a0003c0004t0023g0033a0003c0004t0023g0034others(9): Show | 12 | HG01070.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+4523dupA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83985635 | |||||
chr16:83985745
|
A | G | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.459+4618A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985745 | ||||||
chr16:83985836
|
G | C | 9 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-4658G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985836 | ||||||
chr16:83985911
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.460-4583A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83985911 | ||||||
chr16:83986039
|
G | A | 19 | a0003c0004t0007g0276a0003c0004t0007g0282a0004c0005t0002g0019others(16): Show | 19 | HG00741.hp2 HG01167.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-4455G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986039 | ||||||
chr16:83986039
|
G | T | 3 | a0002c0002t0001g0170a0002c0002t0001g0171a0002c0002t0001g0294 | 3 | HG02015.hp2 NA18957.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.460-4455G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986039 | ||||||
chr16:83986050
|
T | C | 139 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(136): Show | 139 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(136): Show |
intron_variant | MODIFIER | c.460-4444T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986050 | ||||||
chr16:83986052
|
C | T | 1 | a0001c0006t0002g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.460-4442C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986052 | ||||||
chr16:83986119
|
C | A | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-4375C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986119 | ||||||
chr16:83986162
|
G | A | 1 | a0005c0009t0006g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.460-4332G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986162 | ||||||
chr16:83986174
|
G | C | 29 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(26): Show | 29 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-4320G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986174 | ||||||
chr16:83986206
|
G | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.460-4288G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986206 | ||||||
chr16:83986268
|
C | T | 1 | a0003c0004t0023g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.460-4226C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986268 | ||||||
chr16:83986349
|
G | A | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.460-4145G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986349 | ||||||
chr16:83986355
|
T | C | 1 | a0013c0023t0010g0321 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.460-4139T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986355 | ||||||
chr16:83986357
|
C | G | 1 | a0004c0005t0005g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.460-4137C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986357 | ||||||
chr16:83986450
|
T | C | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.460-4044T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986450 | ||||||
chr16:83986456
|
C | T | 1 | a0003c0004t0022g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.460-4038C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986456 | ||||||
chr16:83986501
|
A | G | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.460-3993A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986501 | ||||||
chr16:83986502
|
A | C | 33 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(30): Show | 33 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.460-3992A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986502 | ||||||
chr16:83986503
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.460-3991C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986503 | ||||||
chr16:83986521
|
A | G | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.460-3973A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986521 | ||||||
chr16:83986535
|
C | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.460-3959C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986535 | ||||||
chr16:83986536
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.460-3958G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986536 | ||||||
chr16:83986564
|
G | A | 2 | a0004c0005t0026g0280a0004c0005t0026g0281 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.460-3930G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986564 | ||||||
chr16:83986590
|
G | C | 1 | a0001c0033t0009g0201 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.460-3904G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986590 | ||||||
chr16:83986644
|
C | G | 1 | a0002c0003t0044g0309 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.460-3850C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986644 | ||||||
chr16:83986673
|
C | T | 1 | a0004c0005t0005g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.460-3821C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986673 | ||||||
chr16:83986679
|
A | AT | 19 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(16): Show | 19 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-3795dupT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83986679 | |||||
chr16:83986679
|
AT | A | 34 | a0001c0001t0001g0206a0001c0001t0014g0300a0002c0026t0032g0012others(31): Show | 34 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.460-3795delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83986679 | |||||
chr16:83986679
|
ATT | A | 66 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(63): Show | 66 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(63): Show |
intron_variant | MODIFIER | c.460-3796_460-3795d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83986679 | |||||
chr16:83986679
|
ATTT | A | 8 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0019g0254others(5): Show | 8 | HG01433.hp1 HG01891.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-3797_460-3795d others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83986679 | |||||
chr16:83986753
|
G | C | 137 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(134): Show | 137 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(134): Show |
intron_variant | MODIFIER | c.460-3741G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986753 | ||||||
chr16:83986756
|
G | T | 1 | a0002c0002t0001g0050 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.460-3738G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986756 | ||||||
chr16:83986759
|
A | G | 1 | a0001c0001t0001g0004 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.460-3735A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986759 | ||||||
chr16:83986853
|
G | T | 1 | a0001c0001t0002g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.460-3641G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986853 | ||||||
chr16:83986934
|
A | G | 9 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-3560A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986934 | ||||||
chr16:83986953
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.460-3541C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986953 | ||||||
chr16:83986969
|
G | T | 94 | a0001c0006t0002g0158a0001c0006t0003g0336a0001c0006t0005g0256others(91): Show | 94 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(91): Show |
intron_variant | MODIFIER | c.460-3525G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986969 | ||||||
chr16:83986992
|
A | G | 137 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(134): Show | 137 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(134): Show |
intron_variant | MODIFIER | c.460-3502A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986992 | ||||||
chr16:83986999
|
A | T | 3 | a0002c0026t0032g0012a0003c0016t0020g0216a0004c0036t0005g0214 | 3 | HG02622.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.460-3495A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83986999 | ||||||
chr16:83987014
|
C | A | 2 | a0002c0002t0003g0172a0002c0002t0003g0173 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.460-3480C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987014 | ||||||
chr16:83987029
|
A | G | 25 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(22): Show | 25 | HG00741.hp2 HG01167.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.460-3465A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987029 | ||||||
chr16:83987080
|
G | T | 138 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(135): Show | 138 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(135): Show |
intron_variant | MODIFIER | c.460-3414G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987080 | ||||||
chr16:83987087
|
G | C | 89 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(86): Show | 89 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(86): Show |
intron_variant | MODIFIER | c.460-3407G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987087 | ||||||
chr16:83987186
|
T | G | 9 | a0003c0004t0023g0033a0003c0004t0023g0034a0003c0016t0020g0032others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-3308T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987186 | ||||||
chr16:83987204
|
C | T | 1 | a0002c0002t0013g0104 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.460-3290C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987204 | ||||||
chr16:83987258
|
C | T | 87 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(84): Show | 87 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-3236C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987258 | ||||||
chr16:83987282
|
C | G | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.460-3212C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987282 | ||||||
chr16:83987336
|
G | A | 4 | a0001c0001t0001g0075a0002c0002t0008g0062a0002c0002t0008g0341others(1): Show | 4 | HG00423.hp1 HG02027.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-3158G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987336 | ||||||
chr16:83987385
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0110a0001c0001t0007g0262 | 3 | HG00735.hp1 HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-3109T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987385 | ||||||
chr16:83987417
|
T | C | 1 | a0002c0002t0001g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.460-3077T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987417 | ||||||
chr16:83987449
|
T | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0206a0001c0007t0006g0169others(2): Show | 5 | HG00438.hp2 HG02080.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-3045T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987449 | ||||||
chr16:83987461
|
A | G | 10 | a0002c0026t0032g0012a0003c0004t0023g0033a0003c0004t0023g0034others(7): Show | 10 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-3033A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987461 | ||||||
chr16:83987489
|
C | T | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-3005C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987489 | ||||||
chr16:83987536
|
G | T | 2 | a0002c0002t0003g0172a0002c0002t0003g0173 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.460-2958G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987536 | ||||||
chr16:83987567
|
A | T | 34 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(31): Show | 34 | HG01255.hp2 HG01884.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.460-2927A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987567 | ||||||
chr16:83987606
|
A | AT | 63 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(60): Show | 63 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.460-2882dupT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83987606 | |||||
chr16:83987639
|
T | G | 135 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(132): Show | 135 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(132): Show |
intron_variant | MODIFIER | c.460-2855T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987639 | ||||||
chr16:83987725
|
TATG | T | 30 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(27): Show | 30 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.460-2767_460-2765d others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83987725 | |||||
chr16:83987866
|
T | C | 67 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(64): Show | 67 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(64): Show |
intron_variant | MODIFIER | c.460-2628T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987866 | ||||||
chr16:83987945
|
C | G | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.460-2549C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987945 | ||||||
chr16:83987945
|
C | T | 13 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(10): Show | 13 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.460-2549C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987945 | ||||||
chr16:83987947
|
T | C | 32 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(29): Show | 32 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.460-2547T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83987947 | ||||||
chr16:83988042
|
C | T | 77 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(74): Show | 77 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.460-2452C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988042 | ||||||
chr16:83988044
|
T | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.460-2450T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988044 | ||||||
chr16:83988184
|
C | T | 1 | a0011c0035t0001g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-2310C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988184 | ||||||
chr16:83988209
|
C | T | 3 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316 | 3 | HG02717.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.460-2285C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988209 | ||||||
chr16:83988409
|
C | G | 1 | a0002c0002t0001g0294 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.460-2085C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988409 | ||||||
chr16:83988539
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0027g0106 | 3 | HG01070.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.460-1955C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988539 | ||||||
chr16:83988577
|
G | T | 1 | a0013c0023t0010g0321 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.460-1917G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988577 | ||||||
chr16:83988584
|
G | C | 77 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(74): Show | 77 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.460-1910G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988584 | ||||||
chr16:83988620
|
C | G | 1 | a0002c0003t0010g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.460-1874C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988620 | ||||||
chr16:83988646
|
C | G | 3 | a0001c0006t0003g0336a0001c0006t0005g0256a0002c0003t0031g0310 | 3 | HG02055.hp2 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.460-1848C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988646 | ||||||
chr16:83988659
|
A | G | 1 | a0003c0004t0007g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.460-1835A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988659 | ||||||
chr16:83988665
|
T | G | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1829T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988665 | ||||||
chr16:83988832
|
C | A | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-1662C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988832 | ||||||
chr16:83988837
|
C | CA | 138 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(135): Show | 138 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(135): Show |
intron_variant | MODIFIER | c.460-1657_460-1656i others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988837 | ||||||
chr16:83988837
|
C | G | 1 | a0001c0001t0002g0191 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.460-1657C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988837 | ||||||
chr16:83988880
|
C | T | 24 | a0001c0001t0001g0086a0001c0001t0001g0107a0001c0001t0001g0110others(21): Show | 24 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-1614C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988880 | ||||||
chr16:83988892
|
C | A | 3 | a0008c0014t0003g0194a0008c0014t0003g0320a0008c0014t0038g0236 | 3 | HG02257.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-1602C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988892 | ||||||
chr16:83988960
|
C | A | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1534C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988960 | ||||||
chr16:83988977
|
C | T | 61 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(58): Show | 61 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(58): Show |
intron_variant | MODIFIER | c.460-1517C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83988977 | ||||||
chr16:83989007
|
G | C | 15 | a0003c0004t0003g0035a0003c0004t0003g0245a0003c0004t0003g0247others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-1487G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989007 | ||||||
chr16:83989025
|
T | C | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.460-1469T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989025 | ||||||
chr16:83989126
|
A | G | 1 | a0007c0017t0006g0109 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.460-1368A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989126 | ||||||
chr16:83989173
|
G | A | 5 | a0003c0008t0004g0036a0003c0008t0004g0208a0003c0008t0004g0209others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1321G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989173 | ||||||
chr16:83989192
|
C | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-1302C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989192 | ||||||
chr16:83989237
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-1257G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989237 | ||||||
chr16:83989242
|
C | T | 31 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(28): Show | 31 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.460-1252C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989242 | ||||||
chr16:83989316
|
C | T | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460-1178C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989316 | ||||||
chr16:83989336
|
T | A | 138 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(135): Show | 138 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(135): Show |
intron_variant | MODIFIER | c.460-1158T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989336 | ||||||
chr16:83989368
|
T | A | 2 | a0001c0001t0002g0105a0002c0020t0003g0228 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.460-1126T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989368 | ||||||
chr16:83989383
|
C | G | 2 | a0001c0001t0002g0105a0002c0020t0003g0228 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.460-1111C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989383 | ||||||
chr16:83989413
|
T | C | 5 | a0004c0005t0005g0263a0004c0005t0005g0268a0004c0005t0005g0270others(2): Show | 5 | NA18953.hp1 NA18977.hp1 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-1081T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989413 | ||||||
chr16:83989459
|
C | G | 1 | a0001c0001t0049g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.460-1035C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989459 | ||||||
chr16:83989531
|
A | C | 39 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(36): Show | 39 | HG01255.hp2 HG01433.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.460-963A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989531 | ||||||
chr16:83989533
|
A | T | 39 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(36): Show | 39 | HG01255.hp2 HG01433.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.460-961A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989533 | ||||||
chr16:83989579
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.460-915A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989579 | ||||||
chr16:83989629
|
A | G | 1 | a0002c0002t0001g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.460-865A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989629 | ||||||
chr16:83989652
|
C | G | 43 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(40): Show | 43 | HG01255.hp2 HG01433.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.460-842C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989652 | ||||||
chr16:83989659
|
G | C | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460-835G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989659 | ||||||
chr16:83989786
|
G | C | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.460-708G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989786 | ||||||
chr16:83989813
|
A | G | 43 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(40): Show | 43 | HG01255.hp2 HG01433.hp1 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.460-681A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989813 | ||||||
chr16:83989881
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.460-613C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989881 | ||||||
chr16:83989892
|
A | G | 8 | a0003c0016t0020g0032a0003c0016t0020g0216a0004c0013t0017g0217others(5): Show | 8 | HG02257.hp2 HG02965.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-602A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989892 | ||||||
chr16:83989915
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.460-579C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989915 | ||||||
chr16:83989916
|
G | A | 2 | a0001c0006t0002g0022a0001c0006t0002g0023 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.460-578G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989916 | ||||||
chr16:83989939
|
C | G | 5 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-555C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989939 | ||||||
chr16:83989969
|
T | C | 58 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(55): Show | 58 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(55): Show |
intron_variant | MODIFIER | c.460-525T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989969 | ||||||
chr16:83989995
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.460-499A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83989995 | ||||||
chr16:83990027
|
G | A | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460-467G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990027 | ||||||
chr16:83990094
|
A | G | 1 | a0005c0027t0045g0288 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.460-400A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990094 | ||||||
chr16:83990285
|
AGGGTTCA others(5): Show |
A | 1 | a0003c0008t0004g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.460-206_460-195del others(12): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr16 | 83990285 | |||||
chr16:83990319
|
T | C | 31 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(28): Show | 31 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.460-175T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990319 | ||||||
chr16:83990362
|
C | T | 64 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(61): Show | 64 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.460-132C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990362 | ||||||
chr16:83990367
|
G | A | 16 | a0002c0026t0032g0012a0003c0004t0010g0234a0003c0004t0010g0235others(13): Show | 16 | HG01099.hp1 HG01433.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.460-127G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990367 | ||||||
chr16:83990403
|
C | T | 2 | a0003c0004t0021g0239a0003c0004t0021g0244 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.460-91C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990403 | ||||||
chr16:83990427
|
G | T | 11 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(8): Show | 11 | HG01255.hp1 HG01496.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-67G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990427 | ||||||
chr16:83990439
|
C | A | 1 | a0002c0003t0003g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.460-55C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 5/12 | chr16 | 83990439 | ||||||
chr16:83990670
|
C | T | 10 | a0003c0016t0020g0032a0003c0016t0020g0216a0004c0005t0005g0251others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.596+40C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990670 | ||||||
chr16:83990681
|
C | T | 56 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(53): Show | 56 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(53): Show |
intron_variant | MODIFIER | c.596+51C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990681 | ||||||
chr16:83990682
|
A | G | 10 | a0003c0016t0020g0032a0003c0016t0020g0216a0004c0005t0005g0251others(7): Show | 10 | HG02109.hp2 HG02257.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.596+52A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990682 | ||||||
chr16:83990683
|
C | T | 1 | a0002c0002t0001g0074 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.596+53C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990683 | ||||||
chr16:83990689
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.596+59C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990689 | ||||||
chr16:83990801
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.596+171A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990801 | ||||||
chr16:83990925
|
A | G | 2 | a0002c0003t0012g0325a0002c0003t0012g0326 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.596+295A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990925 | ||||||
chr16:83990927
|
C | A | 4 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.596+297C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990927 | ||||||
chr16:83990930
|
C | G | 1 | a0002c0003t0004g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.596+300C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990930 | ||||||
chr16:83990947
|
C | T | 3 | a0001c0001t0001g0054a0002c0002t0001g0073a0002c0002t0001g0207 | 3 | HG00735.hp2 HG01069.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.596+317C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990947 | ||||||
chr16:83990968
|
C | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.596+338C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990968 | ||||||
chr16:83990990
|
A | T | 28 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(25): Show | 28 | HG00741.hp2 HG01167.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.596+360A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83990990 | ||||||
chr16:83991016
|
C | T | 10 | a0002c0002t0001g0068a0002c0002t0047g0030a0002c0003t0003g0264others(7): Show | 10 | HG02080.hp1 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.596+386C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991016 | ||||||
chr16:83991017
|
G | A | 17 | a0002c0026t0032g0012a0003c0004t0010g0234a0003c0004t0010g0235others(14): Show | 17 | HG01099.hp1 HG01433.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+387G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991017 | ||||||
chr16:83991036
|
C | T | 9 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+406C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991036 | ||||||
chr16:83991060
|
C | T | 2 | a0001c0006t0003g0336a0001c0006t0005g0256 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.596+430C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991060 | ||||||
chr16:83991115
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.596+485T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991115 | ||||||
chr16:83991218
|
C | T | 2 | a0002c0002t0001g0171a0003c0004t0023g0034 | 2 | HG01884.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.596+588C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991218 | ||||||
chr16:83991257
|
A | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.596+627A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991257 | ||||||
chr16:83991309
|
C | G | 58 | a0001c0001t0016g0258a0001c0006t0002g0158a0001c0006t0003g0336others(55): Show | 58 | HG01255.hp1 HG01257.hp2 HG01258.hp1 others(55): Show |
intron_variant | MODIFIER | c.596+679C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991309 | ||||||
chr16:83991330
|
G | A | 1 | a0002c0002t0008g0069 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.596+700G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991330 | ||||||
chr16:83991365
|
TTTC | T | 37 | a0003c0004t0003g0243a0003c0004t0003g0245a0003c0004t0003g0247others(34): Show | 37 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(34): Show |
intron_variant | MODIFIER | c.596+738_596+740del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991365 | |||||
chr16:83991366
|
TTC | T | 40 | a0002c0003t0010g0221a0002c0003t0012g0238a0002c0003t0012g0325others(37): Show | 40 | HG00741.hp2 HG01099.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.596+738_596+739del others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991366 | |||||
chr16:83991367
|
TC | T | 53 | a0001c0001t0016g0258a0001c0006t0003g0336a0001c0006t0005g0256others(50): Show | 53 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.596+738delC | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991367 | ||||||
chr16:83991368
|
C | T | 16 | a0001c0006t0002g0158a0002c0003t0003g0007a0002c0003t0003g0304others(13): Show | 16 | HG01257.hp2 HG01258.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+738C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991368 | ||||||
chr16:83991418
|
G | C | 32 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(29): Show | 32 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.596+788G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991418 | ||||||
chr16:83991427
|
C | T | 3 | a0008c0014t0003g0194a0008c0014t0003g0320a0008c0014t0038g0236 | 3 | HG02257.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.596+797C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991427 | ||||||
chr16:83991448
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0005g0284a0001c0001t0007g0285others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.596+818C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991448 | ||||||
chr16:83991469
|
C | T | 3 | a0001c0001t0002g0056a0002c0003t0004g0337a0003c0004t0030g0329 | 3 | HG02004.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.596+839C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991469 | ||||||
chr16:83991514
|
C | A | 13 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+884C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991514 | ||||||
chr16:83991596
|
C | T | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.596+966C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991596 | ||||||
chr16:83991601
|
C | T | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.596+971C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991601 | ||||||
chr16:83991667
|
GAC | G | 13 | a0003c0004t0007g0276a0003c0004t0007g0282a0004c0005t0005g0263others(10): Show | 13 | HG02074.hp2 HG02132.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.596+1041_596+1042d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991667 | |||||
chr16:83991689
|
C | G | 3 | a0007c0017t0006g0109a0007c0017t0014g0287a0007c0025t0006g0157 | 3 | NA18962.hp2 NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.596+1059C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991689 | ||||||
chr16:83991709
|
C | T | 9 | a0003c0016t0020g0032a0003c0016t0020g0216a0004c0013t0017g0217others(6): Show | 9 | HG02257.hp2 HG02965.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.596+1079C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991709 | ||||||
chr16:83991777
|
G | C | 2 | a0001c0001t0002g0189a0002c0002t0001g0076 | 2 | HG00438.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.596+1147G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991777 | ||||||
chr16:83991789
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.596+1159G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991789 | ||||||
chr16:83991792
|
A | C | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.596+1162A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991792 | ||||||
chr16:83991816
|
A | AT | 36 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0011g0342others(33): Show | 36 | HG00438.hp2 HG00735.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.596+1206dupT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991816 | |||||
chr16:83991816
|
A | ATT | 11 | a0001c0001t0001g0347a0002c0003t0012g0238a0002c0003t0012g0325others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.596+1205_596+1206d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991816 | |||||
chr16:83991816
|
AT | A | 58 | a0001c0001t0001g0061a0001c0001t0002g0052a0001c0001t0002g0346others(55): Show | 58 | HG00741.hp2 HG01099.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.596+1206delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83991816 | |||||
chr16:83991844
|
C | G | 16 | a0002c0026t0032g0012a0003c0004t0010g0234a0003c0004t0010g0235others(13): Show | 16 | HG01099.hp1 HG01433.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.596+1214C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991844 | ||||||
chr16:83991848
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0002g0193 | 2 | HG00280.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.596+1218G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991848 | ||||||
chr16:83991852
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.596+1222C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991852 | ||||||
chr16:83991853
|
G | A | 3 | a0008c0014t0003g0194a0008c0014t0003g0320a0008c0014t0038g0236 | 3 | HG02257.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.596+1223G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991853 | ||||||
chr16:83991855
|
C | T | 7 | a0003c0016t0020g0032a0004c0013t0017g0217a0004c0013t0017g0218others(4): Show | 7 | HG02257.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+1225C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83991855 | ||||||
chr16:83992011
|
C | G | 1 | a0012c0024t0004g0331 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.596+1381C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992011 | ||||||
chr16:83992014
|
G | A | 4 | a0001c0001t0001g0127a0003c0004t0008g0225a0003c0004t0008g0226others(1): Show | 4 | HG02055.hp1 HG03579.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1384G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992014 | ||||||
chr16:83992014
|
G | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.596+1384G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992014 | ||||||
chr16:83992027
|
G | C | 37 | a0003c0004t0003g0035a0003c0004t0003g0245a0003c0004t0003g0247others(34): Show | 37 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.596+1397G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992027 | ||||||
chr16:83992060
|
C | T | 37 | a0003c0004t0003g0035a0003c0004t0003g0245a0003c0004t0003g0247others(34): Show | 37 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.596+1430C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992060 | ||||||
chr16:83992120
|
TGGG | T | 83 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(80): Show | 83 | HG00597.hp2 HG01099.hp1 HG01255.hp1 others(80): Show |
intron_variant | MODIFIER | c.596+1494_596+1496d others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992120 | |||||
chr16:83992204
|
T | C | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.596+1574T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992204 | ||||||
chr16:83992205
|
G | GGT | 161 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(158): Show | 161 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(158): Show |
intron_variant | MODIFIER | c.596+1575_596+1576i others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992205 | ||||||
chr16:83992206
|
T | G | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.596+1576T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992206 | ||||||
chr16:83992209
|
C | CTCACAA | 161 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(158): Show | 161 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(158): Show |
intron_variant | MODIFIER | c.596+1580_596+1581i others(8): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992209 | |||||
chr16:83992209
|
C | T | 1 | a0006c0012t0015g0014 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.596+1579C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992209 | ||||||
chr16:83992211
|
T | A | 161 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(158): Show | 161 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(158): Show |
intron_variant | MODIFIER | c.596+1581T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992211 | ||||||
chr16:83992309
|
T | C | 1 | a0003c0028t0034g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.596+1679T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992309 | ||||||
chr16:83992335
|
C | T | 33 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(30): Show | 33 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.596+1705C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992335 | ||||||
chr16:83992357
|
C | T | 1 | a0002c0003t0012g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.596+1727C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992357 | ||||||
chr16:83992377
|
T | TC | 14 | a0001c0001t0001g0086a0001c0001t0001g0127a0001c0001t0001g0152others(11): Show | 14 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.596+1753dupC | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCC | 16 | a0003c0004t0003g0249a0003c0004t0003g0252a0003c0004t0008g0226others(13): Show | 16 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+1752_596+1753d others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCCCC | 20 | a0003c0004t0003g0245a0003c0004t0007g0276a0003c0004t0007g0282others(17): Show | 20 | HG01167.hp2 HG01943.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.596+1750_596+1753d others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCCCCA | 7 | a0002c0002t0003g0176a0002c0011t0004g0291a0002c0011t0004g0292others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+1751_596+1752i others(7): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCCCCAC | 38 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0002g0193others(35): Show | 38 | HG01255.hp1 HG01496.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.596+1751_596+1752i others(8): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCCCCACC | 28 | a0001c0001t0001g0144a0001c0001t0002g0191a0001c0001t0016g0258others(25): Show | 28 | HG00597.hp2 HG00609.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.596+1751_596+1752i others(9): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TCCCCC | 19 | a0003c0004t0003g0247a0003c0004t0004g0257a0003c0004t0023g0034others(16): Show | 19 | HG00741.hp2 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+1749_596+1753d others(7): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992377 | |||||
chr16:83992377
|
T | TTCCCC | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.596+1747_596+1748i others(7): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992377 | ||||||
chr16:83992378
|
C | A | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.596+1748C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992378 | ||||||
chr16:83992379
|
C | G | 2 | a0001c0001t0001g0082a0001c0033t0009g0201 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.596+1749C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992379 | ||||||
chr16:83992384
|
G | A | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.596+1754G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992384 | ||||||
chr16:83992384
|
G | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(344): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.596+1754G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992384 | ||||||
chr16:83992386
|
C | CCG | 4 | a0003c0004t0003g0243a0003c0004t0003g0248a0003c0004t0040g0018others(1): Show | 4 | HG01255.hp2 HG02109.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.596+1757_596+1758i others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992386 | |||||
chr16:83992407
|
A | T | 1 | a0003c0008t0004g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.596+1777A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992407 | ||||||
chr16:83992517
|
C | T | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.597-1785C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992517 | ||||||
chr16:83992585
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0006g0089a0001c0001t0009g0137others(1): Show | 4 | HG01192.hp2 HG01515.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-1717G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992585 | ||||||
chr16:83992604
|
G | A | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-1698G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992604 | ||||||
chr16:83992636
|
G | C | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-1666G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992636 | ||||||
chr16:83992657
|
T | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.597-1645T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992657 | ||||||
chr16:83992659
|
A | C | 1 | a0001c0001t0002g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.597-1643A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992659 | ||||||
chr16:83992671
|
T | A | 3 | a0002c0002t0001g0136a0002c0002t0001g0162a0002c0002t0001g0187 | 3 | HG00558.hp1 NA18983.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.597-1631T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992671 | ||||||
chr16:83992685
|
G | A | 1 | a0002c0003t0010g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.597-1617G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992685 | ||||||
chr16:83992819
|
T | C | 1 | a0002c0002t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.597-1483T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992819 | ||||||
chr16:83992845
|
C | T | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.597-1457C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992845 | ||||||
chr16:83992855
|
A | G | 2 | a0003c0004t0033g0297a0003c0016t0020g0216 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.597-1447A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992855 | ||||||
chr16:83992935
|
G | C | 17 | a0002c0026t0032g0012a0003c0004t0010g0234a0003c0004t0010g0235others(14): Show | 17 | HG01099.hp1 HG01433.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.597-1367G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992935 | ||||||
chr16:83992940
|
T | TA | 15 | a0003c0004t0003g0249a0003c0004t0003g0250a0003c0004t0003g0252others(12): Show | 15 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.597-1361dupA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83992940 | |||||
chr16:83992951
|
A | G | 1 | a0003c0004t0022g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.597-1351A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992951 | ||||||
chr16:83992966
|
C | T | 1 | a0003c0004t0007g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.597-1336C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992966 | ||||||
chr16:83992994
|
C | T | 76 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(73): Show | 76 | HG00597.hp2 HG00609.hp2 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.597-1308C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83992994 | ||||||
chr16:83993006
|
C | T | 33 | a0003c0004t0003g0035a0003c0004t0007g0276a0003c0004t0007g0282others(30): Show | 33 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.597-1296C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993006 | ||||||
chr16:83993032
|
C | G | 1 | a0003c0028t0034g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.597-1270C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993032 | ||||||
chr16:83993059
|
C | T | 2 | a0003c0004t0022g0295a0003c0008t0004g0210 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.597-1243C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993059 | ||||||
chr16:83993093
|
C | T | 1 | a0003c0008t0004g0036 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.597-1209C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993093 | ||||||
chr16:83993117
|
C | T | 1 | a0002c0002t0001g0197 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.597-1185C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993117 | ||||||
chr16:83993175
|
G | T | 13 | a0004c0018t0001g0040a0004c0018t0001g0302a0004c0037t0006g0145others(10): Show | 13 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.597-1127G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993175 | ||||||
chr16:83993207
|
G | GC | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.597-1094dupC | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993207 | |||||
chr16:83993219
|
G | T | 20 | a0003c0004t0007g0276a0003c0004t0007g0282a0004c0005t0002g0019others(17): Show | 20 | HG00741.hp2 HG01167.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.597-1083G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993219 | ||||||
chr16:83993247
|
C | T | 3 | a0002c0011t0004g0291a0002c0011t0004g0292a0002c0011t0004g0293 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.597-1055C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993247 | ||||||
chr16:83993299
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.597-1003C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993299 | ||||||
chr16:83993340
|
C | G | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-962C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993340 | ||||||
chr16:83993345
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.597-957C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993345 | ||||||
chr16:83993387
|
G | A | 28 | a0003c0004t0003g0243a0003c0004t0003g0245a0003c0004t0003g0247others(25): Show | 28 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.597-915G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993387 | ||||||
chr16:83993411
|
C | T | 73 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(70): Show | 73 | HG00597.hp2 HG00609.hp2 HG01255.hp1 others(70): Show |
intron_variant | MODIFIER | c.597-891C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993411 | ||||||
chr16:83993454
|
C | G | 61 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(58): Show | 61 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.597-848C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993454 | ||||||
chr16:83993571
|
T | C | 31 | a0003c0004t0003g0243a0003c0004t0003g0245a0003c0004t0003g0247others(28): Show | 31 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.597-731T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993571 | ||||||
chr16:83993576
|
C | T | 71 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(68): Show | 71 | HG00597.hp2 HG00609.hp2 HG01255.hp1 others(68): Show |
intron_variant | MODIFIER | c.597-726C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993576 | ||||||
chr16:83993620
|
C | CTG | 41 | a0001c0001t0001g0061a0001c0001t0001g0082a0001c0001t0001g0143others(38): Show | 41 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.597-634_597-633dup others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
C | CTGTG | 15 | a0001c0001t0001g0085a0001c0001t0001g0196a0001c0001t0001g0347others(12): Show | 15 | HG01255.hp1 HG01496.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.597-636_597-633dup others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTG | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0021others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.597-634_597-633del others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTG | C | 39 | a0001c0001t0001g0099a0001c0001t0001g0115a0001c0001t0002g0045others(36): Show | 39 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.597-636_597-633del others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTG | C | 11 | a0001c0001t0001g0181a0001c0001t0056g0114a0001c0006t0002g0025others(8): Show | 11 | HG01261.hp2 HG01943.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.597-638_597-633del others(6): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0001g0107a0001c0001t0002g0042a0002c0003t0008g0027others(7): Show | 10 | HG00099.hp1 HG01515.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.597-640_597-633del others(8): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(3): Show |
C | 9 | a0002c0003t0003g0307a0003c0004t0003g0247a0003c0008t0004g0036others(6): Show | 9 | HG02132.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.597-642_597-633del others(10): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(5): Show |
C | 16 | a0003c0004t0003g0243a0003c0004t0003g0245a0003c0004t0003g0248others(13): Show | 16 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.597-644_597-633del others(12): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(7): Show |
C | 5 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(2): Show | 5 | HG02145.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.597-646_597-633del others(14): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(9): Show |
C | 2 | a0002c0002t0001g0059a0002c0003t0003g0335 | 2 | HG02083.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.597-648_597-633del others(16): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(11): Show |
C | 1 | a0004c0005t0046g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.597-650_597-633del others(18): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(13): Show |
C | 1 | a0004c0005t0041g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.597-652_597-633del others(20): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993620
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0053g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.597-654_597-633del others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 83993620 | |||||
chr16:83993638
|
G | T | 2 | a0002c0002t0047g0030a0002c0003t0004g0315 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.597-664G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993638 | ||||||
chr16:83993744
|
G | C | 61 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(58): Show | 61 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.597-558G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993744 | ||||||
chr16:83993810
|
C | T | 1 | a0013c0023t0010g0321 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.597-492C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993810 | ||||||
chr16:83993862
|
G | C | 1 | a0002c0002t0047g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.597-440G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993862 | ||||||
chr16:83993875
|
C | G | 30 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.597-427C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993875 | ||||||
chr16:83993881
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0094a0001c0001t0001g0128others(3): Show | 7 | NA18954.hp2 NA18955.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.597-421C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993881 | ||||||
chr16:83993974
|
G | A | 31 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(28): Show | 31 | HG01243.hp2 HG01255.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.597-328G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993974 | ||||||
chr16:83993979
|
C | T | 62 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(59): Show | 62 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.597-323C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83993979 | ||||||
chr16:83994012
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.597-290C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994012 | ||||||
chr16:83994024
|
C | T | 1 | a0004c0005t0005g0279 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.597-278C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994024 | ||||||
chr16:83994044
|
G | A | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.597-258G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994044 | ||||||
chr16:83994089
|
T | C | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.597-213T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994089 | ||||||
chr16:83994180
|
G | A | 2 | a0003c0004t0003g0249a0003c0004t0003g0252 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.597-122G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994180 | ||||||
chr16:83994230
|
G | T | 13 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.597-72G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994230 | ||||||
chr16:83994262
|
C | A | 6 | a0002c0003t0003g0264a0002c0003t0003g0265a0002c0003t0003g0266others(3): Show | 6 | HG02559.hp1 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-40C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 6/12 | chr16 | 83994262 | ||||||
chr16:83994449
|
G | A | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.715+29G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/12 | chr16 | 83994449 | ||||||
chr16:83994483
|
C | T | 18 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220others(15): Show | 18 | HG01099.hp1 HG01433.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.715+63C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/12 | chr16 | 83994483 | ||||||
chr16:83994499
|
G | C | 64 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(61): Show | 64 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.715+79G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/12 | chr16 | 83994499 | ||||||
chr16:83994518
|
T | C | 165 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(162): Show | 165 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(162): Show |
intron_variant | MODIFIER | c.716-91T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/12 | chr16 | 83994518 | ||||||
chr16:83994576
|
A | G | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.716-33A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 7/12 | chr16 | 83994576 | ||||||
chr16:83994823
|
G | A | 4 | a0002c0002t0047g0030a0002c0003t0004g0314a0002c0003t0004g0315others(1): Show | 4 | HG02717.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+135G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994823 | ||||||
chr16:83994884
|
G | T | 24 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.795+196G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994884 | ||||||
chr16:83994887
|
C | G | 30 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.795+199C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994887 | ||||||
chr16:83994898
|
G | A | 2 | a0001c0006t0003g0336a0001c0006t0005g0256 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.795+210G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994898 | ||||||
chr16:83994925
|
C | T | 1 | a0013c0023t0010g0321 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.795+237C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994925 | ||||||
chr16:83994926
|
A | G | 91 | a0001c0001t0005g0284a0001c0006t0005g0275a0001c0006t0005g0277others(88): Show | 91 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.795+238A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994926 | ||||||
chr16:83994998
|
C | G | 1 | a0004c0005t0016g0009 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.795+310C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83994998 | ||||||
chr16:83995000
|
A | G | 1 | a0006c0012t0003g0312 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.795+312A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995000 | ||||||
chr16:83995041
|
T | C | 1 | a0001c0006t0005g0275 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.795+353T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995041 | ||||||
chr16:83995044
|
G | T | 3 | a0007c0017t0006g0109a0007c0017t0014g0287a0007c0025t0006g0157 | 3 | NA18962.hp2 NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.795+356G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995044 | ||||||
chr16:83995067
|
A | G | 163 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(160): Show | 163 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(160): Show |
intron_variant | MODIFIER | c.795+379A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995067 | ||||||
chr16:83995097
|
A | G | 162 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(159): Show | 162 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(159): Show |
intron_variant | MODIFIER | c.795+409A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995097 | ||||||
chr16:83995201
|
A | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.795+513A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995201 | ||||||
chr16:83995248
|
G | C | 66 | a0001c0006t0005g0275a0001c0006t0005g0277a0003c0004t0003g0035others(63): Show | 66 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.795+560G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995248 | ||||||
chr16:83995287
|
G | A | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.795+599G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995287 | ||||||
chr16:83995291
|
C | G | 58 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(55): Show | 58 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.795+603C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995291 | ||||||
chr16:83995318
|
C | T | 4 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0004t0037g0313others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+630C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995318 | ||||||
chr16:83995385
|
TAATC | T | 30 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(27): Show | 30 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.795+700_795+703del others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 83995385 | |||||
chr16:83995400
|
C | T | 64 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(61): Show | 64 | HG00597.hp2 HG00609.hp2 HG01257.hp2 others(61): Show |
intron_variant | MODIFIER | c.795+712C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995400 | ||||||
chr16:83995434
|
C | T | 1 | a0002c0002t0001g0195 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.795+746C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995434 | ||||||
chr16:83995479
|
G | A | 2 | a0003c0004t0033g0297a0003c0016t0020g0216 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.795+791G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995479 | ||||||
chr16:83995534
|
T | C | 63 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(60): Show | 63 | HG00597.hp2 HG00609.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.795+846T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995534 | ||||||
chr16:83995553
|
C | G | 62 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(59): Show | 62 | HG00597.hp2 HG00609.hp2 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.795+865C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995553 | ||||||
chr16:83995576
|
C | T | 1 | a0002c0002t0001g0065 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.795+888C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995576 | ||||||
chr16:83995611
|
C | G | 1 | a0012c0024t0004g0331 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.795+923C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995611 | ||||||
chr16:83995639
|
C | T | 1 | a0004c0005t0005g0269 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.795+951C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995639 | ||||||
chr16:83995664
|
C | T | 36 | a0002c0003t0022g0231a0003c0004t0007g0276a0003c0004t0007g0282others(33): Show | 36 | HG00741.hp2 HG01167.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.795+976C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995664 | ||||||
chr16:83995755
|
A | C | 94 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(91): Show | 94 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(91): Show |
intron_variant | MODIFIER | c.795+1067A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995755 | ||||||
chr16:83995756
|
G | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.795+1068G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995756 | ||||||
chr16:83995779
|
G | C | 61 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(58): Show | 61 | HG00597.hp2 HG00609.hp2 HG01257.hp2 others(58): Show |
intron_variant | MODIFIER | c.795+1091G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995779 | ||||||
chr16:83995781
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.795+1093G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995781 | ||||||
chr16:83995803
|
C | T | 3 | a0007c0017t0006g0109a0007c0017t0014g0287a0007c0025t0006g0157 | 3 | NA18962.hp2 NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.795+1115C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995803 | ||||||
chr16:83995839
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.795+1151C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995839 | ||||||
chr16:83995858
|
C | A | 1 | a0001c0001t0002g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.795+1170C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995858 | ||||||
chr16:83995867
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.795+1179G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995867 | ||||||
chr16:83995878
|
G | T | 1 | a0002c0003t0004g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.795+1190G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995878 | ||||||
chr16:83995924
|
C | G | 1 | a0001c0001t0050g0098 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.795+1236C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995924 | ||||||
chr16:83995929
|
G | A | 2 | a0004c0005t0002g0019a0004c0005t0027g0020 | 2 | HG01167.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.795+1241G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995929 | ||||||
chr16:83995949
|
C | T | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.795+1261C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995949 | ||||||
chr16:83995951
|
C | T | 132 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(129): Show | 132 | HG00597.hp2 HG00609.hp2 HG00741.hp2 others(129): Show |
intron_variant | MODIFIER | c.795+1263C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83995951 | ||||||
chr16:83996044
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-1172C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996044 | ||||||
chr16:83996048
|
C | T | 57 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(54): Show | 57 | HG00597.hp2 HG00609.hp2 HG01884.hp2 others(54): Show |
intron_variant | MODIFIER | c.796-1168C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996048 | ||||||
chr16:83996104
|
C | T | 1 | a0004c0005t0010g0237 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.796-1112C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996104 | ||||||
chr16:83996214
|
C | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-1002C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996214 | ||||||
chr16:83996218
|
C | G | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.796-998C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996218 | ||||||
chr16:83996223
|
G | C | 5 | a0002c0003t0003g0264a0002c0003t0003g0265a0002c0003t0003g0266others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-993G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996223 | ||||||
chr16:83996233
|
C | A | 13 | a0001c0007t0006g0215a0004c0018t0001g0040a0004c0037t0006g0145others(10): Show | 13 | HG01081.hp2 HG01099.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.796-983C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996233 | ||||||
chr16:83996239
|
C | A | 26 | a0001c0001t0002g0101a0003c0004t0007g0276a0003c0004t0007g0282others(23): Show | 26 | HG00741.hp2 HG01167.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.796-977C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996239 | ||||||
chr16:83996246
|
A | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-970A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996246 | ||||||
chr16:83996252
|
G | A | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796-964G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996252 | ||||||
chr16:83996399
|
T | C | 14 | a0001c0007t0006g0215a0004c0018t0001g0040a0004c0018t0001g0302others(11): Show | 14 | HG01081.hp2 HG01099.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.796-817T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996399 | ||||||
chr16:83996400
|
T | A | 3 | a0003c0004t0008g0225a0003c0004t0008g0226a0003c0004t0008g0227 | 3 | HG02055.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.796-816T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996400 | ||||||
chr16:83996425
|
C | G | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.796-791C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996425 | ||||||
chr16:83996429
|
C | G | 1 | a0003c0004t0037g0313 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.796-787C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996429 | ||||||
chr16:83996446
|
G | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.796-770G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996446 | ||||||
chr16:83996474
|
C | G | 33 | a0002c0003t0003g0296a0003c0004t0003g0035a0003c0004t0003g0243others(30): Show | 33 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.796-742C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996474 | ||||||
chr16:83996527
|
C | G | 1 | a0012c0024t0004g0331 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.796-689C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996527 | ||||||
chr16:83996597
|
A | T | 14 | a0001c0001t0001g0049a0001c0001t0001g0082a0001c0001t0001g0083others(11): Show | 14 | HG00735.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.796-619A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996597 | ||||||
chr16:83996602
|
GAC | G | 41 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.796-609_796-608del others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 83996602 | |||||
chr16:83996607
|
A | C | 2 | a0004c0005t0026g0280a0004c0005t0026g0281 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.796-609A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996607 | ||||||
chr16:83996617
|
G | C | 13 | a0004c0018t0001g0040a0004c0018t0001g0302a0004c0037t0006g0145others(10): Show | 13 | HG01099.hp1 HG01928.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.796-599G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996617 | ||||||
chr16:83996632
|
A | C | 13 | a0003c0004t0007g0276a0003c0004t0007g0282a0004c0005t0005g0263others(10): Show | 13 | HG02074.hp2 HG02132.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.796-584A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996632 | ||||||
chr16:83996637
|
C | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.796-579C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996637 | ||||||
chr16:83996660
|
C | T | 4 | a0002c0026t0032g0012a0003c0004t0003g0243a0003c0004t0003g0248others(1): Show | 4 | HG01255.hp2 HG02622.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.796-556C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996660 | ||||||
chr16:83996674
|
G | A | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-542G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996674 | ||||||
chr16:83996679
|
A | G | 4 | a0003c0016t0020g0216a0004c0013t0017g0217a0004c0013t0017g0218others(1): Show | 4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-537A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996679 | ||||||
chr16:83996682
|
G | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-534G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996682 | ||||||
chr16:83996684
|
G | A | 48 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.796-532G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996684 | ||||||
chr16:83996697
|
C | T | 2 | a0003c0004t0003g0243a0003c0004t0003g0248 | 2 | HG01255.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.796-519C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996697 | ||||||
chr16:83996735
|
C | T | 193 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.796-481C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996735 | ||||||
chr16:83996761
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.796-455G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996761 | ||||||
chr16:83996764
|
C | T | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-452C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996764 | ||||||
chr16:83996790
|
C | G | 6 | a0002c0003t0004g0260a0002c0003t0004g0261a0002c0003t0012g0238others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.796-426C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996790 | ||||||
chr16:83996814
|
T | G | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-402T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996814 | ||||||
chr16:83996831
|
G | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.796-385G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996831 | ||||||
chr16:83996834
|
T | C | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-382T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996834 | ||||||
chr16:83996851
|
C | T | 1 | a0002c0029t0010g0328 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.796-365C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996851 | ||||||
chr16:83996868
|
C | A | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-348C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996868 | ||||||
chr16:83996951
|
A | C | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-265A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996951 | ||||||
chr16:83996981
|
C | A | 3 | a0002c0002t0001g0136a0002c0002t0001g0162a0002c0002t0001g0187 | 3 | HG00558.hp1 NA18983.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.796-235C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996981 | ||||||
chr16:83996986
|
G | A | 3 | a0001c0001t0002g0346a0001c0001t0011g0344a0001c0001t0011g0345 | 3 | HG02683.hp1 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.796-230G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996986 | ||||||
chr16:83996994
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.796-222C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996994 | ||||||
chr16:83996995
|
C | A | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-221C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83996995 | ||||||
chr16:83997005
|
C | T | 5 | a0002c0003t0003g0264a0002c0003t0003g0265a0002c0003t0003g0266others(2): Show | 5 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.796-211C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997005 | ||||||
chr16:83997034
|
G | A | 4 | a0003c0016t0020g0216a0004c0013t0017g0217a0004c0013t0017g0218others(1): Show | 4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.796-182G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997034 | ||||||
chr16:83997042
|
C | T | 1 | a0001c0001t0011g0200 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.796-174C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997042 | ||||||
chr16:83997045
|
C | T | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-171C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997045 | ||||||
chr16:83997047
|
T | C | 197 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.796-169T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997047 | ||||||
chr16:83997050
|
A | AGGCCCTC others(51): Show |
2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-162_796-161ins others(58): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 83997050 | |||||
chr16:83997055
|
A | G | 1 | a0002c0003t0004g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.796-161A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997055 | ||||||
chr16:83997094
|
C | G | 31 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(28): Show | 31 | HG01243.hp2 HG01255.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.796-122C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997094 | ||||||
chr16:83997111
|
G | A | 1 | a0001c0007t0006g0066 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.796-105G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997111 | ||||||
chr16:83997115
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.796-101C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997115 | ||||||
chr16:83997117
|
T | C | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-99T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997117 | ||||||
chr16:83997152
|
T | G | 3 | a0006c0012t0015g0013a0006c0012t0015g0014a0006c0021t0015g0008 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.796-64T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997152 | ||||||
chr16:83997159
|
T | C | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.796-57T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997159 | ||||||
chr16:83997163
|
C | A | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.796-53C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997163 | ||||||
chr16:83997169
|
G | A | 1 | a0002c0003t0007g0298 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.796-47G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997169 | ||||||
chr16:83997190
|
C | T | 18 | a0003c0004t0003g0249a0003c0004t0003g0250a0003c0004t0003g0252others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.796-26C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997190 | ||||||
chr16:83997193
|
C | G | 3 | a0003c0015t0018g0203a0003c0015t0018g0204a0003c0015t0018g0205 | 3 | HG01257.hp2 HG01258.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.796-23C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 8/12 | chr16 | 83997193 | ||||||
chr16:83997289
|
C | G | 2 | a0002c0002t0001g0160a0002c0002t0001g0161 | 2 | HG02523.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.849+20C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997289 | ||||||
chr16:83997319
|
A | T | 1 | a0004c0005t0005g0270 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.849+50A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997319 | ||||||
chr16:83997344
|
A | G | 3 | a0004c0005t0005g0180a0004c0005t0005g0240a0004c0005t0005g0241 | 3 | HG01433.hp2 HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.849+75A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997344 | ||||||
chr16:83997350
|
C | T | 189 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.849+81C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997350 | ||||||
chr16:83997369
|
C | A | 1 | a0005c0027t0045g0288 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.849+100C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997369 | ||||||
chr16:83997369
|
C | T | 30 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(27): Show | 30 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.849+100C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997369 | ||||||
chr16:83997395
|
C | T | 14 | a0001c0006t0003g0336a0001c0006t0005g0256a0002c0002t0006g0079others(11): Show | 14 | HG02004.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.849+126C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997395 | ||||||
chr16:83997405
|
T | C | 1 | a0001c0006t0002g0028 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.849+136T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997405 | ||||||
chr16:83997414
|
A | C | 2 | a0001c0007t0001g0141a0002c0002t0001g0294 | 2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.849+145A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997414 | ||||||
chr16:83997436
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.849+167C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997436 | ||||||
chr16:83997437
|
C | T | 1 | a0005c0010t0006g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.849+168C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997437 | ||||||
chr16:83997451
|
C | T | 1 | a0004c0005t0041g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.849+182C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997451 | ||||||
chr16:83997452
|
G | A | 1 | a0005c0010t0006g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.849+183G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997452 | ||||||
chr16:83997479
|
C | CT | 44 | a0001c0001t0001g0063a0001c0001t0005g0284a0001c0001t0007g0322others(41): Show | 44 | HG00642.hp2 HG01070.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.849+236dupT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
C | CTT | 34 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.849+235_849+236dup others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
C | CTTT | 8 | a0001c0001t0001g0181a0001c0001t0051g0202a0002c0002t0001g0090others(5): Show | 8 | HG00099.hp2 HG00741.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+234_849+236dup others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
CT | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 158 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.849+236delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
CTT | C | 9 | a0001c0006t0003g0336a0001c0006t0005g0256a0001c0006t0007g0213others(6): Show | 9 | HG02602.hp1 HG02818.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+235_849+236del others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
CTTTT | C | 10 | a0001c0001t0002g0056a0001c0006t0002g0022a0001c0006t0002g0023others(7): Show | 10 | HG01256.hp2 HG01258.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.849+233_849+236del others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997479
|
CTTTTT | C | 13 | a0001c0007t0006g0215a0002c0002t0008g0341a0004c0018t0001g0040others(10): Show | 13 | HG01081.hp2 HG01099.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.849+232_849+236del others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997479 | |||||
chr16:83997514
|
G | C | 5 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(2): Show | 5 | HG01255.hp1 HG01496.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+245G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997514 | ||||||
chr16:83997561
|
T | C | 5 | a0001c0006t0007g0332a0001c0006t0007g0338a0001c0006t0042g0333others(2): Show | 5 | HG01255.hp1 HG01496.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+292T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997561 | ||||||
chr16:83997570
|
C | T | 4 | a0002c0002t0001g0050a0002c0002t0001g0051a0002c0002t0001g0160others(1): Show | 4 | HG02056.hp1 HG02523.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+301C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997570 | ||||||
chr16:83997579
|
C | CTGGGTTC others(74): Show |
4 | a0003c0016t0020g0216a0004c0013t0017g0217a0004c0013t0017g0218others(1): Show | 4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+349_849+350ins others(81): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 83997579 | |||||
chr16:83997586
|
C | T | 30 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(27): Show | 30 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.849+317C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997586 | ||||||
chr16:83997619
|
C | T | 4 | a0003c0016t0020g0216a0004c0013t0017g0217a0004c0013t0017g0218others(1): Show | 4 | HG03209.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+350C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997619 | ||||||
chr16:83997662
|
G | T | 4 | a0001c0006t0007g0338a0001c0006t0042g0333a0002c0026t0032g0012others(1): Show | 4 | HG01255.hp1 HG02622.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+393G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997662 | ||||||
chr16:83997680
|
G | C | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.849+411G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997680 | ||||||
chr16:83997681
|
G | A | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.849+412G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997681 | ||||||
chr16:83997718
|
C | G | 1 | a0004c0005t0005g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.849+449C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997718 | ||||||
chr16:83997721
|
C | G | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.849+452C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997721 | ||||||
chr16:83997731
|
G | T | 1 | a0002c0003t0004g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.849+462G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997731 | ||||||
chr16:83997735
|
T | C | 6 | a0002c0003t0010g0221a0002c0026t0032g0012a0003c0004t0010g0234others(3): Show | 6 | HG01433.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+466T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997735 | ||||||
chr16:83997775
|
G | T | 3 | a0002c0011t0004g0291a0002c0011t0004g0292a0002c0011t0004g0293 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.850-430G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997775 | ||||||
chr16:83997799
|
C | T | 1 | a0001c0001t0011g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.850-406C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997799 | ||||||
chr16:83997830
|
A | G | 86 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.850-375A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997830 | ||||||
chr16:83997846
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0041others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.850-359A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997846 | ||||||
chr16:83997849
|
C | T | 1 | a0002c0003t0007g0308 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.850-356C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997849 | ||||||
chr16:83997850
|
A | G | 42 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(39): Show | 42 | HG00423.hp1 HG00597.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.850-355A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997850 | ||||||
chr16:83997869
|
C | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.850-336C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997869 | ||||||
chr16:83997877
|
A | G | 67 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(64): Show | 67 | HG00423.hp1 HG00597.hp2 HG01123.hp2 others(64): Show |
intron_variant | MODIFIER | c.850-328A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997877 | ||||||
chr16:83997882
|
C | G | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.850-323C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997882 | ||||||
chr16:83997935
|
T | G | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00733.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.850-270T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997935 | ||||||
chr16:83997958
|
G | A | 3 | a0002c0003t0022g0231a0003c0004t0022g0295a0003c0008t0004g0210 | 3 | HG02559.hp2 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.850-247G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83997958 | ||||||
chr16:83998009
|
C | G | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.850-196C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998009 | ||||||
chr16:83998029
|
T | C | 2 | a0002c0002t0029g0029a0002c0003t0044g0309 | 2 | HG02056.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.850-176T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998029 | ||||||
chr16:83998055
|
G | A | 1 | a0003c0004t0021g0239 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.850-150G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998055 | ||||||
chr16:83998070
|
T | G | 28 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(25): Show | 28 | HG01255.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.850-135T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998070 | ||||||
chr16:83998108
|
ATTTTGAC others(4): Show |
A | 14 | a0002c0002t0003g0176a0003c0004t0003g0035a0003c0004t0003g0243others(11): Show | 14 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.850-96_850-86delTT others(9): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998108 | ||||||
chr16:83998117
|
G | A | 164 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0043others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.850-88G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998117 | ||||||
chr16:83998161
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.850-44G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998161 | ||||||
chr16:83998199
|
C | T | 2 | a0004c0005t0026g0280a0004c0005t0026g0281 | 2 | HG03490.hp1 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.850-6C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 9/12 | chr16 | 83998199 | ||||||
chr16:83998331
|
C | T | 18 | a0002c0020t0003g0228a0003c0004t0003g0249a0003c0004t0003g0250others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.962+14C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998331 | ||||||
chr16:83998374
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0196 | 2 | HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.962+57G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998374 | ||||||
chr16:83998378
|
G | A | 1 | a0002c0002t0001g0198 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.962+61G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998378 | ||||||
chr16:83998399
|
T | A | 2 | a0002c0026t0032g0012a0004c0036t0005g0214 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.962+82T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998399 | ||||||
chr16:83998403
|
C | A | 6 | a0002c0003t0003g0229a0002c0003t0003g0264a0002c0003t0003g0265others(3): Show | 6 | HG02559.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.962+86C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998403 | ||||||
chr16:83998418
|
T | C | 138 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(135): Show | 138 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(135): Show |
intron_variant | MODIFIER | c.962+101T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998418 | ||||||
chr16:83998483
|
C | A | 1 | a0002c0002t0001g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.962+166C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998483 | ||||||
chr16:83998506
|
T | C | 83 | a0001c0001t0016g0258a0002c0002t0003g0176a0002c0002t0003g0253others(80): Show | 83 | HG00423.hp1 HG01123.hp2 HG01167.hp1 others(80): Show |
intron_variant | MODIFIER | c.962+189T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998506 | ||||||
chr16:83998530
|
T | C | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.962+213T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998530 | ||||||
chr16:83998535
|
C | T | 3 | a0006c0012t0015g0013a0006c0012t0015g0014a0006c0021t0015g0008 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.962+218C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998535 | ||||||
chr16:83998540
|
G | C | 4 | a0002c0003t0010g0221a0003c0004t0010g0234a0003c0004t0010g0235others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.962+223G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998540 | ||||||
chr16:83998561
|
G | A | 2 | a0003c0016t0020g0032a0003c0016t0020g0216 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.962+244G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998561 | ||||||
chr16:83998594
|
A | C | 2 | a0003c0004t0003g0249a0003c0004t0003g0250 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.962+277A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998594 | ||||||
chr16:83998604
|
G | A | 1 | a0002c0002t0008g0135 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.962+287G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998604 | ||||||
chr16:83998624
|
G | T | 1 | a0001c0006t0005g0256 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.962+307G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998624 | ||||||
chr16:83998650
|
C | G | 1 | a0001c0001t0052g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.962+333C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998650 | ||||||
chr16:83998654
|
C | T | 15 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(12): Show | 15 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.962+337C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998654 | ||||||
chr16:83998655
|
G | A | 22 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(19): Show | 22 | HG01081.hp2 HG01099.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.962+338G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998655 | ||||||
chr16:83998657
|
T | G | 2 | a0002c0002t0001g0059a0002c0002t0001g0179 | 2 | HG02083.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.962+340T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998657 | ||||||
chr16:83998679
|
G | C | 77 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(74): Show | 77 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.962+362G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998679 | ||||||
chr16:83998691
|
C | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.962+374C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998691 | ||||||
chr16:83998705
|
T | C | 30 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(27): Show | 30 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.962+388T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998705 | ||||||
chr16:83998714
|
A | C | 31 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(28): Show | 31 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.962+397A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998714 | ||||||
chr16:83998742
|
T | C | 33 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(30): Show | 33 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.962+425T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998742 | ||||||
chr16:83998796
|
G | GCCATTCT others(2): Show |
5 | a0003c0004t0025g0222a0003c0004t0025g0223a0004c0013t0017g0217others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+481_962+482ins others(9): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83998796 | |||||
chr16:83998801
|
T | C | 5 | a0003c0004t0025g0222a0003c0004t0025g0223a0004c0013t0017g0217others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+484T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998801 | ||||||
chr16:83998801
|
T | TCTCCCCC others(2): Show |
134 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(131): Show | 134 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(131): Show |
intron_variant | MODIFIER | c.962+492_962+493ins others(9): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83998801 | |||||
chr16:83998817
|
T | C | 30 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(27): Show | 30 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.962+500T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998817 | ||||||
chr16:83998824
|
T | C | 3 | a0003c0004t0010g0234a0003c0004t0010g0235a0003c0004t0013g0220 | 3 | HG01433.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.962+507T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998824 | ||||||
chr16:83998827
|
A | C | 30 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(27): Show | 30 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.962+510A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998827 | ||||||
chr16:83998831
|
C | T | 4 | a0002c0003t0010g0221a0003c0004t0010g0234a0003c0004t0010g0235others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.962+514C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998831 | ||||||
chr16:83998832
|
G | A | 3 | a0002c0003t0022g0231a0003c0004t0022g0295a0006c0012t0003g0312 | 3 | HG02559.hp2 HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.962+515G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998832 | ||||||
chr16:83998838
|
A | G | 6 | a0004c0013t0017g0217a0004c0013t0017g0218a0004c0013t0017g0219others(3): Show | 6 | HG02615.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.962+521A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998838 | ||||||
chr16:83998840
|
C | T | 12 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.962+523C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998840 | ||||||
chr16:83998855
|
A | C | 2 | a0001c0001t0001g0060a0001c0001t0002g0081 | 2 | HG02074.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.962+538A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998855 | ||||||
chr16:83998877
|
T | G | 8 | a0002c0002t0003g0176a0002c0002t0003g0253a0002c0002t0003g0255others(5): Show | 8 | HG01255.hp2 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.962+560T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998877 | ||||||
chr16:83998903
|
G | C | 30 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(27): Show | 30 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.962+586G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998903 | ||||||
chr16:83998927
|
G | C | 1 | a0002c0002t0001g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.962+610G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998927 | ||||||
chr16:83998940
|
G | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.962+623G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998940 | ||||||
chr16:83998941
|
A | C | 1 | a0002c0002t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.962+624A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998941 | ||||||
chr16:83998944
|
A | G | 2 | a0002c0002t0008g0341a0002c0002t0013g0340 | 2 | HG00423.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.962+627A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998944 | ||||||
chr16:83998964
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.962+647G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998964 | ||||||
chr16:83998971
|
T | C | 139 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(136): Show | 139 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(136): Show |
intron_variant | MODIFIER | c.962+654T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998971 | ||||||
chr16:83998973
|
C | T | 4 | a0002c0003t0010g0221a0003c0004t0010g0234a0003c0004t0010g0235others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.962+656C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998973 | ||||||
chr16:83998976
|
C | T | 19 | a0001c0006t0005g0256a0002c0002t0047g0030a0002c0003t0003g0224others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.962+659C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998976 | ||||||
chr16:83998993
|
G | C | 136 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(133): Show | 136 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(133): Show |
intron_variant | MODIFIER | c.962+676G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83998993 | ||||||
chr16:83999017
|
C | G | 13 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.962+700C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999017 | ||||||
chr16:83999095
|
A | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.962+778A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999095 | ||||||
chr16:83999117
|
A | G | 19 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.962+800A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999117 | ||||||
chr16:83999177
|
G | C | 1 | a0001c0001t0002g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.962+860G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999177 | ||||||
chr16:83999181
|
G | T | 23 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(20): Show | 23 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.962+864G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999181 | ||||||
chr16:83999184
|
G | A | 5 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+867G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999184 | ||||||
chr16:83999200
|
G | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.962+883G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999200 | ||||||
chr16:83999202
|
A | C | 2 | a0001c0006t0003g0336a0001c0006t0005g0256 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.962+885A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999202 | ||||||
chr16:83999204
|
G | C | 2 | a0001c0006t0007g0332a0001c0006t0042g0333 | 2 | HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.962+887G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999204 | ||||||
chr16:83999209
|
C | T | 29 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(26): Show | 29 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.962+892C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999209 | ||||||
chr16:83999211
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.962+894G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999211 | ||||||
chr16:83999213
|
C | G | 1 | a0002c0002t0003g0253 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.962+896C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999213 | ||||||
chr16:83999225
|
T | C | 56 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(53): Show | 56 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(53): Show |
intron_variant | MODIFIER | c.962+908T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999225 | ||||||
chr16:83999226
|
C | G | 5 | a0002c0003t0012g0238a0002c0003t0012g0325a0002c0003t0012g0326others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+909C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999226 | ||||||
chr16:83999229
|
C | G | 24 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(21): Show | 24 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.962+912C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999229 | ||||||
chr16:83999245
|
C | T | 1 | a0001c0001t0002g0189 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.962+928C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999245 | ||||||
chr16:83999267
|
A | C | 2 | a0002c0003t0004g0260a0002c0003t0004g0261 | 2 | HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.962+950A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999267 | ||||||
chr16:83999268
|
TG | T | 48 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(45): Show | 48 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.962+958delG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83999268 | |||||
chr16:83999282
|
C | A | 1 | a0003c0004t0013g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.962+965C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999282 | ||||||
chr16:83999283
|
C | T | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.962+966C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999283 | ||||||
chr16:83999287
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.962+970C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999287 | ||||||
chr16:83999289
|
A | C | 139 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(136): Show | 139 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(136): Show |
intron_variant | MODIFIER | c.962+972A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999289 | ||||||
chr16:83999332
|
T | G | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.962+1015T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999332 | ||||||
chr16:83999345
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.962+1028C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999345 | ||||||
chr16:83999386
|
C | T | 17 | a0002c0002t0047g0030a0002c0003t0003g0229a0002c0003t0003g0264others(14): Show | 17 | HG01433.hp1 HG01884.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.962+1069C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999386 | ||||||
chr16:83999387
|
G | A | 2 | a0001c0001t0051g0202a0003c0016t0020g0032 | 2 | HG01168.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.962+1070G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999387 | ||||||
chr16:83999416
|
C | T | 1 | a0003c0004t0037g0313 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.962+1099C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999416 | ||||||
chr16:83999446
|
C | T | 20 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(17): Show | 20 | HG01433.hp1 HG02055.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.962+1129C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999446 | ||||||
chr16:83999469
|
A | G | 6 | a0002c0026t0032g0012a0003c0004t0025g0222a0003c0004t0025g0223others(3): Show | 6 | HG01167.hp1 HG01169.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.962+1152A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999469 | ||||||
chr16:83999483
|
A | G | 73 | a0001c0001t0002g0047a0001c0007t0001g0141a0001c0007t0001g0142others(70): Show | 73 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.962+1166A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999483 | ||||||
chr16:83999488
|
T | C | 75 | a0001c0001t0002g0047a0001c0007t0001g0141a0001c0007t0001g0142others(72): Show | 75 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.962+1171T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999488 | ||||||
chr16:83999495
|
C | G | 4 | a0002c0026t0032g0012a0006c0012t0015g0013a0006c0012t0015g0014others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.962+1178C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999495 | ||||||
chr16:83999520
|
A | C | 44 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(41): Show | 44 | HG01081.hp2 HG01099.hp1 HG01884.hp2 others(41): Show |
intron_variant | MODIFIER | c.962+1203A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999520 | ||||||
chr16:83999527
|
G | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963-1197G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999527 | ||||||
chr16:83999541
|
C | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963-1183C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999541 | ||||||
chr16:83999542
|
G | T | 2 | a0002c0003t0004g0230a0002c0003t0004g0232 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.963-1182G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999542 | ||||||
chr16:83999549
|
T | C | 53 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(50): Show | 53 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(50): Show |
intron_variant | MODIFIER | c.963-1175T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999549 | ||||||
chr16:83999550
|
C | T | 3 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316 | 3 | HG02717.hp1 HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.963-1174C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999550 | ||||||
chr16:83999579
|
C | T | 1 | a0001c0001t0009g0096 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.963-1145C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999579 | ||||||
chr16:83999597
|
G | C | 19 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(16): Show | 19 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.963-1127G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999597 | ||||||
chr16:83999624
|
T | C | 2 | a0002c0002t0009g0185a0002c0002t0009g0186 | 2 | NA18955.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.963-1100T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999624 | ||||||
chr16:83999644
|
G | A | 1 | a0002c0002t0008g0062 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.963-1080G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999644 | ||||||
chr16:83999656
|
G | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963-1068G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999656 | ||||||
chr16:83999685
|
C | G | 75 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(72): Show | 75 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.963-1039C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999685 | ||||||
chr16:83999693
|
C | A | 15 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(12): Show | 15 | HG01433.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.963-1031C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999693 | ||||||
chr16:83999693
|
C | T | 1 | a0003c0004t0033g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.963-1031C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999693 | ||||||
chr16:83999718
|
T | C | 54 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(51): Show | 54 | HG00597.hp2 HG01081.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.963-1006T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999718 | ||||||
chr16:83999718
|
T | G | 29 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(26): Show | 29 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.963-1006T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999718 | ||||||
chr16:83999719
|
G | A | 4 | a0002c0003t0003g0224a0002c0003t0010g0330a0002c0003t0010g0334others(1): Show | 4 | HG02055.hp2 HG02258.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.963-1005G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999719 | ||||||
chr16:83999720
|
G | C | 1 | a0003c0004t0004g0257 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.963-1004G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999720 | ||||||
chr16:83999740
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.963-984T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999740 | ||||||
chr16:83999746
|
T | C | 76 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(73): Show | 76 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.963-978T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999746 | ||||||
chr16:83999758
|
C | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.963-966C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999758 | ||||||
chr16:83999829
|
G | C | 18 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(15): Show | 18 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.963-895G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999829 | ||||||
chr16:83999836
|
TAGAA | T | 3 | a0006c0012t0015g0013a0006c0012t0015g0014a0006c0021t0015g0008 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.963-887_963-884del others(4): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999836 | ||||||
chr16:83999859
|
CTTTGATT others(11): Show |
C | 2 | a0008c0014t0003g0194a0008c0014t0003g0320 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.963-841_963-824del others(18): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83999859 | |||||
chr16:83999873
|
GGTT | G | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-850_963-848del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999873 | ||||||
chr16:83999873
|
GGTTTTTT others(14): Show |
G | 1 | a0002c0003t0003g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963-850_963-830del others(21): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999873 | ||||||
chr16:83999882
|
AT | A | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-837delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83999882 | |||||
chr16:83999884
|
T | G | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-840T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999884 | ||||||
chr16:83999885
|
T | A | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-839T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999885 | ||||||
chr16:83999886
|
T | C | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-838T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999886 | ||||||
chr16:83999887
|
T | C | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-837T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999887 | ||||||
chr16:83999891
|
G | T | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-833G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999891 | ||||||
chr16:83999891
|
GGTT | G | 21 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(18): Show | 21 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.963-832_963-830del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999891 | ||||||
chr16:83999892
|
G | C | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-832G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999892 | ||||||
chr16:83999895
|
T | G | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-829T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999895 | ||||||
chr16:83999896
|
T | C | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-828T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999896 | ||||||
chr16:83999899
|
G | A | 3 | a0003c0004t0025g0222a0003c0004t0025g0223a0003c0016t0020g0032 | 3 | HG01167.hp1 HG01169.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.963-825G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999899 | ||||||
chr16:83999899
|
G | T | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-825G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999899 | ||||||
chr16:83999900
|
AGAC | A | 3 | a0002c0003t0003g0264a0002c0003t0003g0266a0002c0003t0003g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.963-823_963-821del others(3): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999900 | ||||||
chr16:83999903
|
C | CCAAATCT others(7): Show |
14 | a0002c0002t0047g0030a0002c0003t0003g0224a0002c0003t0003g0229others(11): Show | 14 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.963-820_963-807dup others(14): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 83999903 | |||||
chr16:83999911
|
T | G | 3 | a0004c0013t0017g0217a0004c0013t0017g0218a0004c0013t0017g0219 | 3 | HG03209.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.963-813T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999911 | ||||||
chr16:83999967
|
A | C | 16 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(13): Show | 16 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.963-757A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999967 | ||||||
chr16:83999988
|
A | G | 21 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(18): Show | 21 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-736A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999988 | ||||||
chr16:83999991
|
A | G | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.963-733A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 83999991 | ||||||
chr16:84000017
|
G | A | 4 | a0002c0003t0003g0224a0003c0004t0025g0222a0003c0004t0025g0223others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.963-707G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000017 | ||||||
chr16:84000023
|
A | T | 1 | a0003c0004t0033g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.963-701A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000023 | ||||||
chr16:84000048
|
A | G | 1 | a0002c0026t0032g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.963-676A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000048 | ||||||
chr16:84000053
|
GTTTTA | G | 21 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(18): Show | 21 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-666_963-662del others(5): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 84000053 | |||||
chr16:84000058
|
AT | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0115others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.963-652delT | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 84000058 | |||||
chr16:84000060
|
T | TTA | 84 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(81): Show | 84 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(81): Show |
intron_variant | MODIFIER | c.963-663_963-662ins others(2): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 84000060 | |||||
chr16:84000061
|
T | TA | 3 | a0002c0002t0008g0062a0002c0002t0008g0341a0003c0015t0018g0204 | 3 | HG01257.hp2 HG02027.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.963-663_963-662ins others(1): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000061 | ||||||
chr16:84000064
|
T | A | 11 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0078others(8): Show | 11 | NA18957.hp1 NA18957.hp2 NA18980.hp1 others(8): Show |
intron_variant | MODIFIER | c.963-660T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000064 | ||||||
chr16:84000066
|
T | A | 21 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(18): Show | 21 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-658T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000066 | ||||||
chr16:84000070
|
T | A | 21 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(18): Show | 21 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-654T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000070 | ||||||
chr16:84000073
|
A | T | 115 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(112): Show | 115 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(112): Show |
intron_variant | MODIFIER | c.963-651A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000073 | ||||||
chr16:84000096
|
T | G | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.963-628T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000096 | ||||||
chr16:84000127
|
C | A | 93 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(90): Show | 93 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(90): Show |
intron_variant | MODIFIER | c.963-597C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000127 | ||||||
chr16:84000168
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.963-556C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000168 | ||||||
chr16:84000172
|
G | C | 21 | a0002c0003t0003g0224a0002c0003t0003g0229a0002c0003t0003g0264others(18): Show | 21 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-552G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000172 | ||||||
chr16:84000181
|
C | T | 90 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(87): Show | 90 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(87): Show |
intron_variant | MODIFIER | c.963-543C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000181 | ||||||
chr16:84000182
|
G | A | 1 | a0003c0004t0033g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.963-542G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000182 | ||||||
chr16:84000184
|
G | A | 4 | a0001c0001t0001g0083a0001c0001t0001g0164a0001c0001t0001g0174others(1): Show | 4 | HG01978.hp1 HG03669.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.963-540G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000184 | ||||||
chr16:84000220
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-504A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000220 | ||||||
chr16:84000221
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-503A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000221 | ||||||
chr16:84000231
|
C | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-493C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000231 | ||||||
chr16:84000234
|
T | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-490T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000234 | ||||||
chr16:84000239
|
T | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-485T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000239 | ||||||
chr16:84000240
|
G | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-484G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000240 | ||||||
chr16:84000250
|
C | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-474C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000250 | ||||||
chr16:84000258
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-466A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000258 | ||||||
chr16:84000260
|
T | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-464T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000260 | ||||||
chr16:84000261
|
G | A | 90 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(87): Show | 90 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(87): Show |
intron_variant | MODIFIER | c.963-463G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000261 | ||||||
chr16:84000262
|
G | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-462G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000262 | ||||||
chr16:84000263
|
C | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-461C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000263 | ||||||
chr16:84000267
|
A | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-457A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000267 | ||||||
chr16:84000273
|
C | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-451C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000273 | ||||||
chr16:84000279
|
T | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-445T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000279 | ||||||
chr16:84000282
|
C | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-442C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000282 | ||||||
chr16:84000294
|
C | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-430C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000294 | ||||||
chr16:84000296
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-428A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000296 | ||||||
chr16:84000297
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-427A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000297 | ||||||
chr16:84000300
|
T | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-424T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000300 | ||||||
chr16:84000302
|
A | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-422A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000302 | ||||||
chr16:84000303
|
G | C | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-421G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000303 | ||||||
chr16:84000304
|
A | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-420A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000304 | ||||||
chr16:84000307
|
A | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-417A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000307 | ||||||
chr16:84000312
|
C | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-412C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000312 | ||||||
chr16:84000317
|
C | G | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-407C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000317 | ||||||
chr16:84000318
|
C | T | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.963-406C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000318 | ||||||
chr16:84000327
|
A | C | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-397A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000327 | ||||||
chr16:84000350
|
CAAGACCC others(23): Show |
C | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-371_963-342del others(30): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 84000350 | |||||
chr16:84000389
|
C | T | 1 | a0001c0001t0056g0114 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.963-335C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000389 | ||||||
chr16:84000401
|
T | A | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-323T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000401 | ||||||
chr16:84000414
|
G | A | 31 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(28): Show | 31 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.963-310G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000414 | ||||||
chr16:84000435
|
A | G | 2 | a0002c0002t0047g0030a0002c0026t0032g0012 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.963-289A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000435 | ||||||
chr16:84000439
|
T | C | 12 | a0003c0004t0003g0035a0003c0004t0003g0243a0003c0004t0003g0245others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.963-285T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000439 | ||||||
chr16:84000469
|
T | A | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.963-255T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000469 | ||||||
chr16:84000470
|
G | C | 1 | a0001c0001t0002g0047 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.963-254G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000470 | ||||||
chr16:84000474
|
C | A | 1 | a0001c0001t0002g0193 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.963-250C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000474 | ||||||
chr16:84000478
|
A | G | 144 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(141): Show | 144 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(141): Show |
intron_variant | MODIFIER | c.963-246A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000478 | ||||||
chr16:84000500
|
G | A | 11 | a0002c0003t0003g0224a0002c0003t0004g0230a0002c0003t0004g0232others(8): Show | 11 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.963-224G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000500 | ||||||
chr16:84000524
|
C | T | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-200C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000524 | ||||||
chr16:84000526
|
G | A | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-198G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000526 | ||||||
chr16:84000547
|
G | T | 2 | a0003c0004t0025g0222a0003c0004t0025g0223 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.963-177G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000547 | ||||||
chr16:84000563
|
C | G | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-161C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000563 | ||||||
chr16:84000570
|
C | T | 2 | a0002c0002t0003g0172a0002c0002t0003g0173 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.963-154C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000570 | ||||||
chr16:84000582
|
T | G | 1 | a0002c0020t0003g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.963-142T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000582 | ||||||
chr16:84000586
|
G | A | 1 | a0002c0003t0012g0238 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.963-138G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000586 | ||||||
chr16:84000591
|
A | T | 1 | a0008c0014t0038g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.963-133A>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000591 | ||||||
chr16:84000624
|
G | A | 1 | a0002c0002t0001g0179 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.963-100G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000624 | ||||||
chr16:84000632
|
T | G | 3 | a0003c0004t0003g0245a0003c0004t0003g0247a0003c0004t0004g0257 | 3 | HG02615.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.963-92T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000632 | ||||||
chr16:84000661
|
A | C | 1 | a0001c0007t0002g0138 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.963-63A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000661 | ||||||
chr16:84000688
|
C | T | 2 | a0002c0002t0001g0179a0002c0002t0008g0093 | 2 | HG02083.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.963-36C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000688 | ||||||
chr16:84000705
|
C | T | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.963-19C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 10/12 | chr16 | 84000705 | ||||||
chr16:84000826
|
GGTGAGGG others(12): Show |
G | 3 | a0006c0012t0015g0013a0006c0012t0015g0014a0006c0021t0015g0008 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1040+29_1040+47del others(19): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84000826 | |||||
chr16:84000829
|
GAGGGAGA others(11): Show |
G | 29 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(26): Show | 29 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1040+29_1040+46del others(18): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000829 | ||||||
chr16:84000834
|
A | G | 79 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(76): Show | 79 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.1040+33A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000834 | ||||||
chr16:84000842
|
G | T | 79 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(76): Show | 79 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.1040+41G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000842 | ||||||
chr16:84000848
|
G | A | 1 | a0004c0005t0005g0246 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1040+47G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000848 | ||||||
chr16:84000881
|
G | A | 1 | a0003c0004t0013g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1040+80G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000881 | ||||||
chr16:84000885
|
G | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040+84G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000885 | ||||||
chr16:84000895
|
G | T | 45 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(42): Show | 45 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.1040+94G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000895 | ||||||
chr16:84000907
|
T | C | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040+106T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000907 | ||||||
chr16:84000908
|
C | G | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.1040+107C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000908 | ||||||
chr16:84000911
|
C | T | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040+110C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000911 | ||||||
chr16:84000919
|
C | G | 1 | a0002c0002t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1040+118C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000919 | ||||||
chr16:84000920
|
G | A | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040+119G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000920 | ||||||
chr16:84000933
|
G | A | 1 | a0006c0021t0015g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1040+132G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000933 | ||||||
chr16:84000947
|
G | A | 4 | a0001c0001t0002g0042a0002c0002t0001g0090a0002c0002t0001g0117others(1): Show | 4 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040+146G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000947 | ||||||
chr16:84000947
|
G | C | 146 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(143): Show | 146 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(143): Show |
intron_variant | MODIFIER | c.1040+146G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000947 | ||||||
chr16:84000956
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0174a0004c0018t0001g0302 | 3 | HG03669.hp1 HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1040+155C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000956 | ||||||
chr16:84000959
|
T | TGGTGGAG | 112 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(109): Show | 112 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(109): Show |
intron_variant | MODIFIER | c.1040+160_1040+166d others(9): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84000959 | |||||
chr16:84000968
|
C | T | 2 | a0003c0004t0025g0222a0003c0004t0025g0223 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1040+167C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000968 | ||||||
chr16:84000974
|
C | T | 3 | a0008c0014t0003g0194a0008c0014t0003g0320a0008c0014t0038g0236 | 3 | HG02257.hp2 HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1040+173C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000974 | ||||||
chr16:84000978
|
T | TG | 109 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(106): Show | 109 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(106): Show |
intron_variant | MODIFIER | c.1040+179dupG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84000978 | |||||
chr16:84000981
|
T | G | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.1040+180T>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000981 | ||||||
chr16:84000987
|
G | C | 6 | a0002c0003t0003g0224a0002c0003t0010g0330a0002c0003t0010g0334others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+186G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84000987 | ||||||
chr16:84001000
|
C | G | 6 | a0002c0003t0003g0224a0002c0003t0010g0330a0002c0003t0010g0334others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+199C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001000 | ||||||
chr16:84001017
|
T | C | 112 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(109): Show | 112 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(109): Show |
intron_variant | MODIFIER | c.1040+216T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001017 | ||||||
chr16:84001063
|
C | G | 66 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(63): Show | 66 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.1040+262C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001063 | ||||||
chr16:84001075
|
G | C | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.1040+274G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001075 | ||||||
chr16:84001086
|
C | T | 1 | a0003c0016t0020g0032 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1040+285C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001086 | ||||||
chr16:84001087
|
G | A | 6 | a0002c0003t0004g0230a0002c0003t0004g0232a0002c0003t0010g0221others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+286G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001087 | ||||||
chr16:84001128
|
A | G | 148 | a0001c0001t0001g0063a0001c0001t0001g0143a0001c0001t0001g0144others(145): Show | 148 | HG00423.hp1 HG00597.hp2 HG01081.hp2 others(145): Show |
intron_variant | MODIFIER | c.1040+327A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001128 | ||||||
chr16:84001130
|
C | T | 12 | a0002c0002t0011g0163a0002c0002t0011g0165a0002c0002t0024g0323others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1040+329C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001130 | ||||||
chr16:84001140
|
G | A | 112 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(109): Show | 112 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(109): Show |
intron_variant | MODIFIER | c.1040+339G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001140 | ||||||
chr16:84001204
|
C | T | 3 | a0004c0013t0017g0217a0004c0013t0017g0218a0004c0013t0017g0219 | 3 | HG03209.hp1 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1040+403C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001204 | ||||||
chr16:84001212
|
G | A | 9 | a0002c0002t0001g0070a0002c0002t0001g0071a0002c0002t0001g0078others(6): Show | 9 | NA18957.hp2 NA18980.hp1 NA18986.hp2 others(6): Show |
intron_variant | MODIFIER | c.1040+411G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001212 | ||||||
chr16:84001219
|
G | T | 1 | a0004c0036t0005g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1040+418G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001219 | ||||||
chr16:84001249
|
TAGGCCTT others(28): Show |
T | 6 | a0002c0003t0004g0230a0002c0003t0004g0232a0002c0003t0010g0221others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1040+452_1040+486d others(37): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84001249 | |||||
chr16:84001251
|
G | A | 1 | a0005c0010t0006g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1040+450G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001251 | ||||||
chr16:84001255
|
TTTGTCCT others(13): Show |
T | 103 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(100): Show | 103 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(100): Show |
intron_variant | MODIFIER | c.1040+455_1040+474d others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001255 | ||||||
chr16:84001265
|
G | A | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1040+464G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001265 | ||||||
chr16:84001308
|
G | A | 28 | a0002c0002t0008g0016a0002c0002t0008g0031a0002c0002t0008g0062others(25): Show | 28 | HG00423.hp1 HG01123.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1040+507G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001308 | ||||||
chr16:84001314
|
C | T | 1 | a0003c0004t0033g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1041-511C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001314 | ||||||
chr16:84001315
|
C | G | 1 | a0002c0002t0001g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1041-510C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001315 | ||||||
chr16:84001331
|
G | A | 109 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(106): Show | 109 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(106): Show |
intron_variant | MODIFIER | c.1041-494G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001331 | ||||||
chr16:84001376
|
A | G | 108 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(105): Show | 108 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(105): Show |
intron_variant | MODIFIER | c.1041-449A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001376 | ||||||
chr16:84001381
|
T | A | 59 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(56): Show | 59 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(56): Show |
intron_variant | MODIFIER | c.1041-444T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001381 | ||||||
chr16:84001384
|
C | T | 1 | a0003c0016t0020g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1041-441C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001384 | ||||||
chr16:84001385
|
G | A | 109 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(106): Show | 109 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(106): Show |
intron_variant | MODIFIER | c.1041-440G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001385 | ||||||
chr16:84001424
|
C | T | 1 | a0004c0005t0005g0278 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1041-401C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001424 | ||||||
chr16:84001425
|
G | A | 7 | a0001c0001t0002g0042a0001c0006t0003g0336a0001c0006t0005g0256others(4): Show | 7 | HG00099.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041-400G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001425 | ||||||
chr16:84001426
|
G | C | 110 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(107): Show | 110 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(107): Show |
intron_variant | MODIFIER | c.1041-399G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001426 | ||||||
chr16:84001432
|
A | G | 110 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(107): Show | 110 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(107): Show |
intron_variant | MODIFIER | c.1041-393A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001432 | ||||||
chr16:84001441
|
A | G | 111 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.1041-384A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001441 | ||||||
chr16:84001458
|
C | T | 22 | a0002c0002t0047g0030a0002c0003t0004g0230a0002c0003t0004g0232others(19): Show | 22 | HG01433.hp1 HG01884.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1041-367C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001458 | ||||||
chr16:84001493
|
G | C | 110 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(107): Show | 110 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(107): Show |
intron_variant | MODIFIER | c.1041-332G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001493 | ||||||
chr16:84001498
|
C | T | 2 | a0002c0003t0003g0304a0002c0003t0003g0319 | 2 | NA19057.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1041-327C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001498 | ||||||
chr16:84001499
|
G | A | 1 | a0002c0002t0001g0160 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1041-326G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001499 | ||||||
chr16:84001499
|
G | T | 91 | a0002c0002t0003g0176a0002c0002t0003g0253a0002c0002t0003g0255others(88): Show | 91 | HG00423.hp1 HG01123.hp2 HG01243.hp2 others(88): Show |
intron_variant | MODIFIER | c.1041-326G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001499 | ||||||
chr16:84001508
|
G | T | 17 | a0002c0002t0047g0030a0002c0003t0004g0315a0002c0003t0012g0238others(14): Show | 17 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1041-317G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001508 | ||||||
chr16:84001509
|
T | C | 114 | a0001c0001t0009g0140a0002c0002t0003g0172a0002c0002t0003g0173others(111): Show | 114 | HG00423.hp1 HG00609.hp1 HG01109.hp1 others(111): Show |
intron_variant | MODIFIER | c.1041-316T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001509 | ||||||
chr16:84001510
|
G | C | 1 | a0002c0003t0004g0337 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1041-315G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001510 | ||||||
chr16:84001533
|
G | T | 1 | a0001c0001t0009g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1041-292G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001533 | ||||||
chr16:84001534
|
A | C | 1 | a0002c0011t0004g0291 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1041-291A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001534 | ||||||
chr16:84001590
|
T | A | 13 | a0001c0001t0016g0258a0002c0003t0003g0229a0002c0003t0003g0264others(10): Show | 13 | HG01243.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1041-235T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001590 | ||||||
chr16:84001591
|
G | A | 27 | a0001c0001t0001g0099a0001c0001t0001g0206a0001c0007t0001g0142others(24): Show | 27 | HG01081.hp2 HG01099.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1041-234G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001591 | ||||||
chr16:84001611
|
T | A | 38 | a0001c0001t0053g0188a0002c0002t0001g0123a0002c0003t0003g0229others(35): Show | 38 | HG00423.hp2 HG01433.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.1041-214T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001611 | ||||||
chr16:84001638
|
T | C | 2 | a0003c0004t0023g0033a0003c0004t0023g0034 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1041-187T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001638 | ||||||
chr16:84001639
|
C | T | 1 | a0001c0001t0052g0166 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1041-186C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001639 | ||||||
chr16:84001663
|
CCCTGGGC others(13): Show |
C | 84 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(81): Show | 84 | HG01109.hp1 HG01123.hp2 HG01243.hp1 others(81): Show |
intron_variant | MODIFIER | c.1041-159_1041-140d others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84001663 | |||||
chr16:84001675
|
CCTCACCT others(13): Show |
C | 5 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-147_1041-128d others(22): Show |
NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 84001675 | |||||
chr16:84001684
|
C | T | 1 | a0001c0001t0009g0096 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1041-141C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001684 | ||||||
chr16:84001709
|
C | T | 10 | a0002c0003t0022g0231a0002c0011t0004g0291a0002c0011t0004g0292others(7): Show | 10 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1041-116C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001709 | ||||||
chr16:84001715
|
G | A | 107 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(104): Show | 107 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(104): Show |
intron_variant | MODIFIER | c.1041-110G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001715 | ||||||
chr16:84001729
|
G | A | 60 | a0002c0002t0003g0176a0002c0002t0003g0253a0002c0002t0003g0255others(57): Show | 60 | HG00423.hp1 HG01123.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.1041-96G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001729 | ||||||
chr16:84001730
|
C | G | 2 | a0004c0005t0005g0278a0004c0005t0005g0283 | 2 | NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1041-95C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001730 | ||||||
chr16:84001743
|
G | T | 108 | a0002c0002t0003g0172a0002c0002t0003g0173a0002c0002t0003g0176others(105): Show | 108 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(105): Show |
intron_variant | MODIFIER | c.1041-82G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001743 | ||||||
chr16:84001753
|
G | A | 5 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-72G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001753 | ||||||
chr16:84001773
|
C | G | 1 | a0003c0004t0010g0235 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1041-52C>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001773 | ||||||
chr16:84001775
|
C | T | 15 | a0002c0003t0003g0224a0002c0003t0004g0230a0002c0003t0004g0232others(12): Show | 15 | HG01884.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1041-50C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001775 | ||||||
chr16:84001790
|
G | A | 3 | a0006c0012t0015g0013a0006c0012t0015g0014a0006c0021t0015g0008 | 3 | HG02615.hp1 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1041-35G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001790 | ||||||
chr16:84001796
|
C | T | 1 | a0002c0002t0011g0163 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1041-29C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001796 | ||||||
chr16:84001803
|
C | A | 5 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-22C>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 11/12 | chr16 | 84001803 | ||||||
chr16:84001919
|
A | AG | 5 | a0002c0003t0004g0314a0002c0003t0004g0315a0002c0003t0004g0316others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132+8dupG | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr16 | 84001919 | |||||
chr16:84001926
|
A | G | 111 | a0001c0001t0011g0120a0001c0001t0011g0200a0001c0001t0011g0342others(108): Show | 111 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(108): Show |
intron_variant | MODIFIER | c.1132+10A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84001926 | ||||||
chr16:84001937
|
A | C | 19 | a0001c0007t0001g0141a0001c0007t0001g0142a0001c0007t0001g0149others(16): Show | 19 | HG01081.hp2 HG02015.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.1132+21A>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84001937 | ||||||
chr16:84001989
|
A | G | 114 | a0001c0001t0011g0120a0001c0001t0011g0200a0001c0001t0011g0342others(111): Show | 114 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(111): Show |
intron_variant | MODIFIER | c.1132+73A>G | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84001989 | ||||||
chr16:84002059
|
G | C | 1 | a0002c0002t0047g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1132+143G>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002059 | ||||||
chr16:84002109
|
C | T | 4 | a0002c0003t0010g0221a0003c0004t0010g0234a0003c0004t0010g0235others(1): Show | 4 | HG01433.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132+193C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002109 | ||||||
chr16:84002126
|
G | A | 6 | a0002c0003t0004g0230a0002c0003t0004g0232a0002c0003t0010g0221others(3): Show | 6 | HG01433.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1133-192G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002126 | ||||||
chr16:84002126
|
G | T | 1 | a0002c0002t0047g0030 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1133-192G>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002126 | ||||||
chr16:84002157
|
C | T | 4 | a0002c0002t0047g0030a0003c0004t0033g0297a0003c0016t0020g0032others(1): Show | 4 | HG02809.hp2 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1133-161C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002157 | ||||||
chr16:84002225
|
C | CA | 24 | a0001c0001t0006g0089a0001c0001t0014g0300a0001c0001t0014g0301others(21): Show | 24 | HG01081.hp2 HG01099.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1133-92dupA | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr16 | 84002225 | |||||
chr16:84002227
|
T | A | 24 | a0001c0001t0006g0089a0001c0001t0014g0300a0001c0001t0014g0301others(21): Show | 24 | HG01081.hp2 HG01099.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.1133-91T>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002227 | ||||||
chr16:84002233
|
G | A | 116 | a0001c0001t0011g0120a0001c0001t0011g0200a0001c0001t0011g0342others(113): Show | 116 | HG00423.hp1 HG01109.hp1 HG01123.hp2 others(113): Show |
intron_variant | MODIFIER | c.1133-85G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002233 | ||||||
chr16:84002239
|
T | C | 143 | a0001c0001t0006g0089a0001c0001t0011g0120a0001c0001t0011g0200others(140): Show | 143 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(140): Show |
intron_variant | MODIFIER | c.1133-79T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002239 | ||||||
chr16:84002249
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1133-69C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002249 | ||||||
chr16:84002295
|
C | T | 2 | a0003c0004t0023g0033a0003c0004t0023g0034 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1133-23C>T | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002295 | ||||||
chr16:84002300
|
G | A | 2 | a0004c0013t0017g0218a0004c0013t0017g0219 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1133-18G>A | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002300 | ||||||
chr16:84002314
|
T | C | 148 | a0001c0001t0002g0081a0001c0001t0002g0155a0001c0001t0006g0089others(145): Show | 148 | HG00423.hp1 HG01081.hp2 HG01099.hp1 others(145): Show |
splice_region_variant&intron_variant | LOW | c.1133-4T>C | NECAB2 | ENSG00000103154.10 | transcript | ENST00000305202.9 | protein_coding | 12/12 | chr16 | 84002314 |