geneid | 11199 |
---|---|
ensemblid | ENSG00000109511.12 |
hgncid | 534 |
symbol | ANXA10 |
name | annexin A10 |
refseq_nuc | NM_007193.5 |
refseq_prot | NP_009124.2 |
ensembl_nuc | ENST00000359299.8 |
ensembl_prot | ENSP00000352248.3 |
mane_status | MANE Select |
chr | chr4 |
start | 168092537 |
end | 168187736 |
strand | + |
ver | v1.2 |
region | chr4:168092537-168187736 |
region5000 | chr4:168087537-168192736 |
regionname0 | ANXA10_chr4_168092537_168187736 |
regionname5000 | ANXA10_chr4_168087537_168192736 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 324 | 158 | 65 | 35 | 31 | 8 | 18 | 27 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0002 | 1/0 | 324 | 111 | 21 | 17 | 56 | 4 | 12 | 47 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0003 | 0/0 | 324 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0004 | 0/0 | 324 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0005 | 0/0 | 324 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0006 | 0/0 | 324 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0007 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 975 | 128 | 56 | 27 | 26 | 4 | 15 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0002 | 1/0 | 975 | 110 | 20 | 17 | 56 | 4 | 12 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0003 | 0/1 | 975 | 25 | 8 | 7 | 3 | 3 | 3 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0004 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0005 | 0/0 | 975 | 4 | 0 | 0 | 4 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0006 | 0/0 | 975 | 3 | 0 | 1 | 0 | 0 | 2 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0007 | 0/0 | 975 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0008 | 0/0 | 975 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0009 | 0/0 | 975 | 2 | 0 | 1 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0010 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0011 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
c0012 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 467 | 284 | 92 | 54 | 92 | 12 | 32 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 975 | 128 | 56 | 27 | 26 | 4 | 15 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0003 | 0/1 | 975 | 25 | 8 | 7 | 3 | 3 | 3 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0008 | 0/0 | 975 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0009 | 0/0 | 975 | 2 | 0 | 1 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0011 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0002c0002 | 1/0 | 975 | 110 | 20 | 17 | 56 | 4 | 12 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0002c0012 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0003c0004 | 0/0 | 975 | 5 | 5 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0004c0005 | 0/0 | 975 | 4 | 0 | 0 | 4 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0005c0006 | 0/0 | 975 | 3 | 0 | 1 | 0 | 0 | 2 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0006c0007 | 0/0 | 975 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0007c0010 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1441 | 128 | 56 | 27 | 26 | 4 | 15 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0003t0001 | 0/1 | 1441 | 25 | 8 | 7 | 3 | 3 | 3 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0008t0001 | 0/0 | 1441 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0009t0001 | 0/0 | 1441 | 2 | 0 | 1 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0001c0011t0001 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0002c0002t0001 | 1/0 | 1441 | 110 | 20 | 17 | 56 | 4 | 12 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0002c0012t0001 | 0/0 | 1441 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0003c0004t0001 | 0/0 | 1441 | 5 | 5 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0004c0005t0001 | 0/0 | 1441 | 4 | 0 | 0 | 4 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0005c0006t0001 | 0/0 | 1441 | 3 | 0 | 1 | 0 | 0 | 2 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0006c0007t0001 | 0/0 | 1441 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
a0007c0010t0001 | 0/0 | 1441 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | copy fasta | chr4 | 168087537 | 168192736 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0009t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0001c0011t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0002c0012t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0003c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0003c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0003c0004t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0003c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0004c0005t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0004c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0004c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0004c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0005c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0005c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0005c0006t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0006c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0006c0007t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
a0007c0010t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0009 | t0001 | g0208 | EUR | GBR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0130 | EUR | GBR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0013 | EUR | FIN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0162 | EUR | FIN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00423 | hp1 | a0007 | c0010 | t0001 | g0053 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | CHS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00639 | hp2 | a0006 | c0007 | t0001 | g0268 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00741 | hp1 | a0005 | c0006 | t0001 | g0172 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0027 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0142 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0035 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0137 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0034 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01361 | hp2 | a0001 | c0009 | t0001 | g0207 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0257 | EUR | IBS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01515 | hp2 | a0001 | c0003 | t0001 | g0037 | EUR | IBS | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0179 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02004 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02055 | hp2 | a0001 | c0011 | t0001 | g0216 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | CDX | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | CDX | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0197 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0275 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PEL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02572 | hp1 | a0006 | c0007 | t0001 | g0015 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0230 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0022 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0238 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0200 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03130 | hp1 | a0003 | c0004 | t0001 | g0223 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0274 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03453 | hp1 | a0003 | c0004 | t0001 | g0224 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03491 | hp2 | a0005 | c0006 | t0001 | g0118 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03492 | hp1 | a0005 | c0006 | t0001 | g0119 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0109 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0166 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0131 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0023 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0175 | SAS | STU | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0096 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18939 | hp2 | a0001 | c0008 | t0001 | g0248 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18951 | hp1 | a0004 | c0005 | t0001 | g0049 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18974 | hp2 | a0004 | c0005 | t0001 | g0048 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18995 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19002 | hp2 | a0004 | c0005 | t0001 | g0043 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0244 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19063 | hp1 | a0004 | c0005 | t0001 | g0050 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19078 | hp2 | a0001 | c0008 | t0001 | g0247 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | ASW | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ASW | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0120 | EUR | TSI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0025 | EUR | TSI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | GIH | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG03471 | hp2 | a0003 | c0004 | t0001 | g0220 | AFR | MSL | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | USA | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | USA | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | USA | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | USA | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
NA21309 | hp2 | a0002 | c0012 | t0001 | g0113 | AFR | LWK | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0033 | REF | REF | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0204 | REF | REF | ANXA10_chr4_168087537_168192736 | ANXA10 | chr4 | 168087537 | 168192736 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:168139524
|
C | T | 1 | a0005 | 3 | HG00741.hp1 HG03491.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.139C>T | p.Arg47Cys | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/12 | 303/1441 | 139/975 | 47/324 | chr4 | 168139524 | ||
chr4:168162543
|
A | C | 2 | a0001a0003 | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
missense_variant | MODERATE | c.211A>C | p.Met71Leu | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/12 | 375/1441 | 211/975 | 71/324 | chr4 | 168162543 | ||
chr4:168177749
|
G | A | 1 | a0007 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.490G>A | p.Glu164Lys | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 7/12 | 654/1441 | 490/975 | 164/324 | chr4 | 168177749 | ||
chr4:168177932
|
A | C | 1 | a0004 | 4 | NA18951.hp1 NA18974.hp2 NA19002.hp2 others(1): Show |
missense_variant | MODERATE | c.577A>C | p.Thr193Pro | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/12 | 741/1441 | 577/975 | 193/324 | chr4 | 168177932 | ||
chr4:168177938
|
C | G | 1 | a0003 | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
missense_variant | MODERATE | c.583C>G | p.Leu195Val | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/12 | 747/1441 | 583/975 | 195/324 | chr4 | 168177938 | ||
chr4:168179310
|
T | C | 1 | a0006 | 2 | HG00639.hp2 HG02572.hp1 |
missense_variant&splice_region_variant | MODERATE | c.722T>C | p.Ile241Thr | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/12 | 886/1441 | 722/975 | 241/324 | chr4 | 168179310 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:168128161
|
A | T | 2 | a0001c0009a0002c0012 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.96A>T | p.Gly32Gly | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/12 | 260/1441 | 96/975 | 32/324 | chr4 | 168128161 | ||
chr4:168165290
|
A | G | 6 | a0001c0001a0001c0003a0001c0008others(3): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
synonymous_variant | LOW | c.444A>G | p.Ser148Ser | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/12 | 608/1441 | 444/975 | 148/324 | chr4 | 168165290 | ||
chr4:168177763
|
A | G | 2 | a0001c0003a0001c0011 | 26 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
synonymous_variant | LOW | c.504A>G | p.Thr168Thr | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 7/12 | 668/1441 | 504/975 | 168/324 | chr4 | 168177763 | ||
chr4:168177919
|
G | A | 1 | a0001c0011 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.564G>A | p.Thr188Thr | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/12 | 728/1441 | 564/975 | 188/324 | chr4 | 168177919 | ||
chr4:168177974
|
C | T | 1 | a0001c0008 | 2 | NA18939.hp2 NA19078.hp2 |
synonymous_variant | LOW | c.619C>T | p.Leu207Leu | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/12 | 783/1441 | 619/975 | 207/324 | chr4 | 168177974 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:168092923
|
T | G | 1 | a0002c0002t0001g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.18+205T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168092923 | ||||||
chr4:168092962
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.18+244A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168092962 | ||||||
chr4:168092985
|
A | C | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+267A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168092985 | ||||||
chr4:168093044
|
TTCAATAT others(14): Show |
T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+327_18+347delTC others(19): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093044 | ||||||
chr4:168093061
|
A | G | 4 | a0001c0001t0001g0267a0002c0002t0001g0269a0002c0002t0001g0270others(1): Show | 4 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+343A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093061 | ||||||
chr4:168093177
|
T | C | 1 | a0002c0002t0001g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.18+459T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093177 | ||||||
chr4:168093218
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+500T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093218 | ||||||
chr4:168093298
|
TGAATA | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 27 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.18+584_18+588delTA others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168093298 | |||||
chr4:168093374
|
T | C | 13 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+656T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093374 | ||||||
chr4:168093380
|
T | G | 2 | a0001c0001t0001g0039a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.18+662T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093380 | ||||||
chr4:168093382
|
C | T | 2 | a0001c0001t0001g0039a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.18+664C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093382 | ||||||
chr4:168093383
|
A | G | 2 | a0001c0001t0001g0039a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.18+665A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093383 | ||||||
chr4:168093844
|
A | C | 1 | a0002c0002t0001g0266 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.18+1126A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093844 | ||||||
chr4:168093886
|
A | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+1168A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093886 | ||||||
chr4:168093969
|
A | T | 27 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(24): Show | 27 | HG00438.hp2 HG01361.hp1 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.18+1251A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168093969 | ||||||
chr4:168094299
|
A | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(31): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.18+1581A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094299 | ||||||
chr4:168094486
|
G | T | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.18+1768G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094486 | ||||||
chr4:168094518
|
A | C | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.18+1800A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094518 | ||||||
chr4:168094578
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.18+1860T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094578 | ||||||
chr4:168094635
|
T | C | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+1917T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094635 | ||||||
chr4:168094716
|
T | C | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(31): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.18+1998T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094716 | ||||||
chr4:168094799
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+2081T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094799 | ||||||
chr4:168094804
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+2086A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094804 | ||||||
chr4:168094875
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+2157G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094875 | ||||||
chr4:168094890
|
T | G | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+2172T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168094890 | ||||||
chr4:168095107
|
G | A | 2 | a0005c0006t0001g0118a0005c0006t0001g0119 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.18+2389G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095107 | ||||||
chr4:168095109
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0003t0001g0238 | 3 | HG02258.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.18+2391C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095109 | ||||||
chr4:168095199
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.18+2481A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095199 | ||||||
chr4:168095200
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.18+2482G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095200 | ||||||
chr4:168095377
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.18+2659T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095377 | ||||||
chr4:168095452
|
G | A | 2 | a0002c0002t0001g0120a0002c0002t0001g0121 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.18+2734G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095452 | ||||||
chr4:168095541
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.18+2823T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095541 | ||||||
chr4:168095578
|
C | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+2860C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095578 | ||||||
chr4:168095749
|
A | C | 2 | a0001c0001t0001g0039a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.18+3031A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095749 | ||||||
chr4:168095788
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(80): Show | 84 | HG00423.hp1 HG00438.hp2 HG01081.hp2 others(81): Show |
intron_variant | MODIFIER | c.18+3070T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095788 | ||||||
chr4:168095792
|
G | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.18+3074G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095792 | ||||||
chr4:168095951
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.18+3233A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168095951 | ||||||
chr4:168096042
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.18+3324G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096042 | ||||||
chr4:168096072
|
G | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG02622.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.18+3354G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096072 | ||||||
chr4:168096157
|
G | A | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+3439G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096157 | ||||||
chr4:168096379
|
A | G | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.18+3661A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096379 | ||||||
chr4:168096573
|
G | A | 6 | a0001c0001t0001g0267a0001c0003t0001g0038a0002c0002t0001g0269others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+3855G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096573 | ||||||
chr4:168096623
|
T | G | 26 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 27 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.18+3905T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096623 | ||||||
chr4:168096653
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG01081.hp2 HG01255.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.18+3935C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096653 | ||||||
chr4:168096758
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.18+4040A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096758 | ||||||
chr4:168096803
|
C | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+4085C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096803 | ||||||
chr4:168096851
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18+4133C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096851 | ||||||
chr4:168096911
|
C | CAT | 3 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124 | 3 | HG01891.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.18+4210_18+4211dup others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATAT | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+4206_18+4211dup others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(5): Show |
2 | a0001c0001t0001g0004a0001c0001t0001g0199 | 3 | HG02895.hp1 HG02897.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.18+4200_18+4211dup others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(7): Show |
1 | a0002c0002t0001g0040 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.18+4198_18+4211dup others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(9): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0041 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.18+4196_18+4211dup others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(11): Show |
3 | a0001c0001t0001g0235a0002c0002t0001g0115a0002c0002t0001g0234 | 3 | HG02970.hp1 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.18+4194_18+4211dup others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(13): Show |
7 | a0001c0001t0001g0117a0001c0001t0001g0214a0001c0001t0001g0233others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(20): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(15): Show |
5 | a0001c0001t0001g0229a0001c0001t0001g0231a0002c0002t0001g0269others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(22): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(17): Show |
10 | a0001c0001t0001g0005a0001c0001t0001g0213a0001c0001t0001g0225others(7): Show | 11 | HG00639.hp2 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(24): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(19): Show |
11 | a0001c0001t0001g0008a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 11 | HG01891.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(21): Show |
2 | a0001c0001t0001g0218a0001c0001t0001g0237 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(23): Show |
1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(30): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(43): Show |
1 | a0002c0002t0001g0006 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(50): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(41): Show |
1 | a0002c0002t0001g0274 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(48): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(37): Show |
1 | a0001c0001t0001g0271 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(44): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(35): Show |
1 | a0002c0002t0001g0275 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(42): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(33): Show |
1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(31): Show |
1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(38): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096911
|
C | CATATATA others(53): Show |
1 | a0001c0001t0001g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(60): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096911 | |||||
chr4:168096912
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0277 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(58): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096912 | |||||
chr4:168096926
|
A | ATATATAT others(15): Show |
2 | a0001c0003t0001g0013a0001c0003t0001g0014 | 2 | HG00323.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(22): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(20): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(11): Show |
16 | a0001c0001t0001g0031a0001c0003t0001g0020a0001c0003t0001g0021others(13): Show | 16 | HG00741.hp2 HG01074.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0003t0001g0037 | 4 | HG01081.hp1 HG01515.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(34): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(25): Show |
1 | a0004c0005t0001g0043 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(32): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(23): Show |
9 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(6): Show | 9 | HG03139.hp2 HG03225.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(30): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0051 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(23): Show |
1 | a0001c0001t0001g0052 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(30): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(21): Show |
64 | a0001c0001t0001g0002a0001c0001t0001g0054a0001c0001t0001g0055others(61): Show | 65 | HG00423.hp1 HG00738.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(19): Show |
12 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0112others(9): Show | 12 | HG00140.hp1 HG00438.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(17): Show |
1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(24): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(37): Show |
3 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257 | 3 | HG01361.hp1 HG01515.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.18+4211_18+4212ins others(44): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(35): Show |
1 | a0002c0002t0001g0258 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(42): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATATGT others(21): Show |
1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+4211_18+4212ins others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATATGTAT others(19): Show |
1 | a0001c0001t0001g0116 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.18+4215_18+4216ins others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATGTATGT others(21): Show |
5 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+4209_18+4210ins others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096926
|
A | ATGTATGT others(19): Show |
1 | a0001c0001t0001g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.18+4209_18+4210ins others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168096926 | |||||
chr4:168096930
|
G | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG01123.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+4212G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096930 | ||||||
chr4:168096934
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.18+4216G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096934 | ||||||
chr4:168096940
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.18+4222G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096940 | ||||||
chr4:168096979
|
A | G | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+4261A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096979 | ||||||
chr4:168096997
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0229 | 4 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+4279T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168096997 | ||||||
chr4:168097286
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 26 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+4568C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097286 | ||||||
chr4:168097379
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.18+4661C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097379 | ||||||
chr4:168097698
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(13): Show | 17 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.18+4980C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097698 | ||||||
chr4:168097739
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+5021C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097739 | ||||||
chr4:168097770
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+5052G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097770 | ||||||
chr4:168097797
|
C | T | 2 | a0001c0001t0001g0041a0002c0002t0001g0115 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.18+5079C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097797 | ||||||
chr4:168097820
|
A | C | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.18+5102A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168097820 | ||||||
chr4:168098095
|
TTAAATC | T | 5 | a0001c0001t0001g0267a0001c0003t0001g0038a0002c0002t0001g0269others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+5381_18+5386del others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168098095 | |||||
chr4:168098120
|
TA | T | 6 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0273others(3): Show | 6 | HG02258.hp1 HG02273.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+5414delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168098120 | |||||
chr4:168098121
|
A | T | 1 | a0002c0002t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.18+5403A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168098121 | ||||||
chr4:168098161
|
T | C | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+5443T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168098161 | ||||||
chr4:168098235
|
C | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(51): Show | 57 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.18+5517C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168098235 | ||||||
chr4:168098589
|
AAT | A | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG00140.hp1 HG00738.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.18+5873_18+5874del others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168098589 | |||||
chr4:168098716
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(125): Show | 130 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.18+5998A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168098716 | ||||||
chr4:168099102
|
C | T | 13 | a0001c0001t0001g0267a0001c0001t0001g0271a0001c0001t0001g0272others(10): Show | 14 | HG00639.hp2 HG01109.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.18+6384C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168099102 | ||||||
chr4:168099330
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0253a0002c0002t0001g0115 | 3 | HG02976.hp1 NA19030.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.18+6612C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168099330 | ||||||
chr4:168099415
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(53): Show | 57 | HG00423.hp1 HG01081.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.18+6697G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168099415 | ||||||
chr4:168099705
|
T | C | 1 | a0002c0002t0001g0125 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.18+6987T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168099705 | ||||||
chr4:168099892
|
A | T | 1 | a0001c0003t0001g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.18+7174A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168099892 | ||||||
chr4:168100154
|
C | G | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+7436C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168100154 | ||||||
chr4:168100181
|
T | A | 1 | a0001c0003t0001g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.18+7463T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168100181 | ||||||
chr4:168100465
|
C | T | 1 | a0002c0002t0001g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.18+7747C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168100465 | ||||||
chr4:168100665
|
C | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+7947C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168100665 | ||||||
chr4:168100851
|
TC | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+8136delC | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168100851 | |||||
chr4:168100914
|
A | G | 1 | a0001c0003t0001g0034 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.18+8196A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168100914 | ||||||
chr4:168101071
|
G | A | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.18+8353G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101071 | ||||||
chr4:168101102
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0209others(25): Show | 30 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.18+8384G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101102 | ||||||
chr4:168101235
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.18+8517C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101235 | ||||||
chr4:168101491
|
G | GT | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0002c0002t0001g0195others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+8781dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168101491 | |||||
chr4:168101567
|
T | C | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(4): Show | 7 | HG00423.hp1 NA18939.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.18+8849T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101567 | ||||||
chr4:168101630
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(39): Show | 45 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.18+8912G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101630 | ||||||
chr4:168101696
|
T | A | 2 | a0002c0002t0001g0125a0002c0002t0001g0126 | 2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.18+8978T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101696 | ||||||
chr4:168101749
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(39): Show | 45 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.18+9031T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101749 | ||||||
chr4:168101794
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0017others(132): Show | 137 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.18+9076A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101794 | ||||||
chr4:168101962
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18952.hp1 NA18991.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+9244A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168101962 | ||||||
chr4:168102159
|
T | C | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.18+9441T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102159 | ||||||
chr4:168102164
|
A | G | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.18+9446A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102164 | ||||||
chr4:168102235
|
G | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+9517G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102235 | ||||||
chr4:168102495
|
T | C | 1 | a0002c0002t0001g0269 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.18+9777T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102495 | ||||||
chr4:168102629
|
G | A | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.18+9911G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102629 | ||||||
chr4:168102745
|
TG | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0055others(1): Show | 5 | HG01106.hp1 HG01261.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.18+10028delG | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102745 | ||||||
chr4:168102787
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.18+10069A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102787 | ||||||
chr4:168102842
|
C | G | 1 | a0002c0002t0001g0269 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.18+10124C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102842 | ||||||
chr4:168102923
|
A | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(181): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.18+10205A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102923 | ||||||
chr4:168102979
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+10261G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168102979 | ||||||
chr4:168103072
|
G | A | 1 | a0002c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.18+10354G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103072 | ||||||
chr4:168103310
|
G | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0273 | 2 | HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.18+10592G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103310 | ||||||
chr4:168103312
|
C | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+10594C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103312 | ||||||
chr4:168103431
|
C | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(31): Show | 36 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.18+10713C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103431 | ||||||
chr4:168103507
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.18+10789G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103507 | ||||||
chr4:168103536
|
G | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(39): Show | 45 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.18+10818G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103536 | ||||||
chr4:168103556
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+10838C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103556 | ||||||
chr4:168103597
|
C | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+10879C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103597 | ||||||
chr4:168103914
|
C | T | 5 | a0001c0001t0001g0267a0001c0003t0001g0038a0002c0002t0001g0269others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+11196C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168103914 | ||||||
chr4:168104065
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.18+11347A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168104065 | ||||||
chr4:168104313
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+11595G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168104313 | ||||||
chr4:168104388
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.18+11670A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168104388 | ||||||
chr4:168104547
|
A | G | 5 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0278others(2): Show | 5 | HG00099.hp1 HG01123.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+11829A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168104547 | ||||||
chr4:168104609
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.18+11891A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168104609 | ||||||
chr4:168104839
|
CTTGTCT | C | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.18+12124_18+12129d others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168104839 | |||||
chr4:168105069
|
A | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.18+12351A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105069 | ||||||
chr4:168105328
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.18+12610T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105328 | ||||||
chr4:168105360
|
A | G | 1 | a0002c0002t0001g0191 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.18+12642A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105360 | ||||||
chr4:168105372
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(99): Show | 103 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.18+12654T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105372 | ||||||
chr4:168105424
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+12706A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105424 | ||||||
chr4:168105449
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.18+12731A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105449 | ||||||
chr4:168105462
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.18+12744G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105462 | ||||||
chr4:168105478
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.18+12760T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105478 | ||||||
chr4:168105532
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.18+12814A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105532 | ||||||
chr4:168105586
|
A | T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+12868A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168105586 | ||||||
chr4:168106006
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+13288T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106006 | ||||||
chr4:168106144
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+13426T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106144 | ||||||
chr4:168106169
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+13451G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106169 | ||||||
chr4:168106213
|
A | G | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.18+13495A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106213 | ||||||
chr4:168106430
|
T | C | 1 | a0002c0002t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.18+13712T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106430 | ||||||
chr4:168106858
|
T | C | 3 | a0001c0003t0001g0013a0001c0003t0001g0016a0001c0003t0001g0020 | 3 | HG00323.hp1 HG02559.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.18+14140T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168106858 | ||||||
chr4:168107356
|
C | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(19): Show | 23 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.18+14638C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168107356 | ||||||
chr4:168107457
|
T | G | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.18+14739T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168107457 | ||||||
chr4:168107703
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.18+14985T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168107703 | ||||||
chr4:168107743
|
G | A | 1 | a0001c0003t0001g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.18+15025G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168107743 | ||||||
chr4:168107859
|
T | C | 1 | a0002c0002t0001g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.18+15141T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168107859 | ||||||
chr4:168108001
|
G | A | 26 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(23): Show | 27 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.18+15283G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108001 | ||||||
chr4:168108013
|
G | A | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | NA18960.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.18+15295G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108013 | ||||||
chr4:168108017
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.18+15299A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108017 | ||||||
chr4:168108383
|
T | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.18+15665T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108383 | ||||||
chr4:168108673
|
CT | C | 27 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0209others(24): Show | 29 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.18+15956delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108673 | ||||||
chr4:168108709
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.18+15991G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108709 | ||||||
chr4:168108781
|
G | T | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.18+16063G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108781 | ||||||
chr4:168108937
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.18+16219C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168108937 | ||||||
chr4:168109383
|
T | G | 5 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG02559.hp2 HG02976.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.18+16665T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168109383 | ||||||
chr4:168109577
|
A | G | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+16859A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168109577 | ||||||
chr4:168109584
|
C | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.18+16866C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168109584 | ||||||
chr4:168109677
|
A | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(136): Show | 142 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.18+16959A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168109677 | ||||||
chr4:168109800
|
A | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | NA18970.hp1 NA19011.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.18+17082A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168109800 | ||||||
chr4:168110005
|
T | C | 6 | a0002c0002t0001g0132a0002c0002t0001g0133a0002c0002t0001g0134others(3): Show | 6 | NA18941.hp2 NA18943.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.18+17287T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110005 | ||||||
chr4:168110028
|
G | A | 4 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02451.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.18+17310G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110028 | ||||||
chr4:168110136
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.18+17418G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110136 | ||||||
chr4:168110196
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0229others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+17478G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110196 | ||||||
chr4:168110244
|
T | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0229others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.18+17526T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110244 | ||||||
chr4:168110252
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.18+17534C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110252 | ||||||
chr4:168110444
|
C | CT | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-17624dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168110444 | |||||
chr4:168110794
|
A | G | 2 | a0002c0002t0001g0136a0002c0002t0001g0266 | 2 | NA19057.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.19-17290A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110794 | ||||||
chr4:168110820
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.19-17264C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110820 | ||||||
chr4:168110964
|
C | A | 2 | a0002c0002t0001g0125a0002c0002t0001g0126 | 2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.19-17120C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168110964 | ||||||
chr4:168111117
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.19-16967A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111117 | ||||||
chr4:168111169
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.19-16915G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111169 | ||||||
chr4:168111332
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0003t0001g0013others(4): Show | 8 | HG00323.hp1 HG01081.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-16752A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111332 | ||||||
chr4:168111651
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.19-16433C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111651 | ||||||
chr4:168111690
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(130): Show | 136 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.19-16394A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111690 | ||||||
chr4:168111745
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-16339T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111745 | ||||||
chr4:168111805
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-16279A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111805 | ||||||
chr4:168111843
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00639.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.19-16241T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111843 | ||||||
chr4:168111904
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0267a0001c0003t0001g0014others(4): Show | 7 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-16180G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168111904 | ||||||
chr4:168112049
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19-16035T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112049 | ||||||
chr4:168112337
|
C | A | 1 | a0002c0002t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.19-15747C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112337 | ||||||
chr4:168112462
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-15622G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112462 | ||||||
chr4:168112463
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-15621T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112463 | ||||||
chr4:168112464
|
T | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-15620T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112464 | ||||||
chr4:168112518
|
T | C | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-15566T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112518 | ||||||
chr4:168112522
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-15562A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112522 | ||||||
chr4:168112545
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.19-15539C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112545 | ||||||
chr4:168112865
|
A | G | 1 | a0002c0002t0001g0131 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.19-15219A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168112865 | ||||||
chr4:168113132
|
C | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-14952C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113132 | ||||||
chr4:168113175
|
A | G | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.19-14909A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113175 | ||||||
chr4:168113191
|
C | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-14893C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113191 | ||||||
chr4:168113263
|
C | CTCTCACT others(31): Show |
36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(33): Show | 38 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.19-14647_19-14610d others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113263 | |||||
chr4:168113263
|
C | CTCTCACT others(69): Show |
4 | a0001c0001t0001g0209a0001c0003t0001g0021a0001c0009t0001g0207others(1): Show | 4 | HG00099.hp1 HG01106.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-14685_19-14610d others(78): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113263 | |||||
chr4:168113263
|
C | CTCTCACT others(31): Show |
1 | a0002c0002t0001g0258 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.19-14802_19-14801i others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113263 | |||||
chr4:168113263
|
C | CTCTCACT others(69): Show |
2 | a0002c0002t0001g0256a0002c0002t0001g0257 | 2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.19-14802_19-14801i others(78): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113263 | |||||
chr4:168113263
|
CTCTCACT others(31): Show |
C | 6 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(3): Show | 6 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-14647_19-14610d others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113263 | |||||
chr4:168113300
|
C | T | 4 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG01891.hp2 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-14784C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113300 | ||||||
chr4:168113348
|
G | GGTCTGGT others(107): Show |
1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.19-14623_19-14622i others(116): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113348 | |||||
chr4:168113348
|
G | GGTCTGGT others(69): Show |
120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(117): Show | 122 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.19-14661_19-14660i others(78): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113348 | |||||
chr4:168113348
|
G | GGTCTGGT others(31): Show |
1 | a0002c0002t0001g0258 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.19-14699_19-14698i others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113348 | |||||
chr4:168113348
|
G | T | 2 | a0002c0002t0001g0256a0002c0002t0001g0257 | 2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.19-14736G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113348 | ||||||
chr4:168113361
|
C | CCCAGTCT others(31): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0231others(1): Show | 4 | HG02145.hp2 HG02572.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-14686_19-14685i others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168113361 | |||||
chr4:168113532
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.19-14552C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113532 | ||||||
chr4:168113544
|
G | A | 1 | a0002c0002t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.19-14540G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113544 | ||||||
chr4:168113587
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.19-14497A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168113587 | ||||||
chr4:168114265
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19-13819A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114265 | ||||||
chr4:168114270
|
T | TATAAATA others(5): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-13811_19-13810i others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168114270 | |||||
chr4:168114339
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG01109.hp2 HG02004.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.19-13745T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114339 | ||||||
chr4:168114485
|
G | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-13599G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114485 | ||||||
chr4:168114653
|
T | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(52): Show | 56 | HG00423.hp1 HG01081.hp2 HG01106.hp1 others(53): Show |
intron_variant | MODIFIER | c.19-13431T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114653 | ||||||
chr4:168114817
|
C | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(177): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.19-13267C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114817 | ||||||
chr4:168114853
|
C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0002c0002t0001g0234 | 3 | HG01123.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.19-13231C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114853 | ||||||
chr4:168114897
|
A | AT | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-13179dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168114897 | |||||
chr4:168114976
|
C | G | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.19-13108C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114976 | ||||||
chr4:168114984
|
C | T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-13100C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168114984 | ||||||
chr4:168115092
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-12992A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115092 | ||||||
chr4:168115103
|
G | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-12981G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115103 | ||||||
chr4:168115476
|
A | G | 11 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0237others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-12608A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115476 | ||||||
chr4:168115495
|
A | ACG | 3 | a0001c0001t0001g0012a0001c0011t0001g0216a0002c0002t0001g0226 | 3 | HG00099.hp2 HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.19-12587_19-12586d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115495 | |||||
chr4:168115497
|
G | GCA | 27 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0046others(24): Show | 28 | HG01106.hp1 HG01261.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.19-12547_19-12546d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
G | GCACA | 10 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0085others(7): Show | 10 | HG01255.hp1 HG03239.hp1 HG03491.hp1 others(7): Show |
intron_variant | MODIFIER | c.19-12549_19-12546d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
G | GCGCACA | 3 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011 | 3 | HG00735.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.19-12586_19-12585i others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCA | G | 61 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(58): Show | 62 | HG00323.hp1 HG00423.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.19-12547_19-12546d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCACA | G | 39 | a0001c0001t0001g0039a0001c0001t0001g0095a0001c0001t0001g0098others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.19-12549_19-12546d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCACACA | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0083others(18): Show | 22 | HG01123.hp2 HG01361.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.19-12551_19-12546d others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCACACAC others(1): Show |
G | 8 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0271others(5): Show | 9 | HG02258.hp1 HG02280.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-12553_19-12546d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCACACAC others(3): Show |
G | 4 | a0001c0001t0001g0276a0001c0001t0001g0277a0002c0002t0001g0115others(1): Show | 4 | HG01109.hp1 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.19-12555_19-12546d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115497
|
GCACACAC others(5): Show |
G | 6 | a0001c0001t0001g0041a0001c0001t0001g0267a0001c0003t0001g0014others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-12557_19-12546d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168115497 | |||||
chr4:168115499
|
A | G | 2 | a0001c0001t0001g0214a0002c0002t0001g0226 | 2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.19-12585A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115499 | ||||||
chr4:168115501
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 22 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.19-12583A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115501 | ||||||
chr4:168115503
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0212a0001c0001t0001g0218others(3): Show | 6 | HG01884.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-12581A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115503 | ||||||
chr4:168115505
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0225a0001c0001t0001g0229others(6): Show | 10 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.19-12579A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115505 | ||||||
chr4:168115507
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0003t0001g0238 | 3 | HG02258.hp1 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.19-12577A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115507 | ||||||
chr4:168115563
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.19-12521G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115563 | ||||||
chr4:168115584
|
T | G | 1 | a0001c0003t0001g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-12500T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115584 | ||||||
chr4:168115807
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.19-12277G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115807 | ||||||
chr4:168115875
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19-12209T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115875 | ||||||
chr4:168115889
|
C | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-12195C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115889 | ||||||
chr4:168115966
|
A | G | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-12118A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115966 | ||||||
chr4:168115989
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.19-12095C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115989 | ||||||
chr4:168115996
|
C | T | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19-12088C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168115996 | ||||||
chr4:168116014
|
A | T | 1 | a0001c0003t0001g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.19-12070A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116014 | ||||||
chr4:168116055
|
G | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-12029G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116055 | ||||||
chr4:168116087
|
C | CA | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-11989dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168116087 | |||||
chr4:168116133
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG02622.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-11951T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116133 | ||||||
chr4:168116207
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(39): Show | 44 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.19-11877T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116207 | ||||||
chr4:168116287
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0229others(2): Show | 6 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.19-11797G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116287 | ||||||
chr4:168116342
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(115): Show | 120 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19-11742T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116342 | ||||||
chr4:168116584
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18952.hp1 NA18991.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-11500A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116584 | ||||||
chr4:168116595
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(115): Show | 120 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19-11489T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116595 | ||||||
chr4:168116733
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19-11351T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116733 | ||||||
chr4:168116813
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-11271T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116813 | ||||||
chr4:168116962
|
G | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-11122G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168116962 | ||||||
chr4:168116996
|
G | GACACACA others(3): Show |
7 | a0001c0001t0001g0278a0002c0002t0001g0122a0002c0002t0001g0123others(4): Show | 7 | HG01891.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-11083_19-11074d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168116996 | |||||
chr4:168116996
|
G | GACACACA others(5): Show |
131 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(128): Show | 134 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.19-11085_19-11074d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168116996 | |||||
chr4:168116996
|
G | GACACACA others(7): Show |
17 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.19-11087_19-11074d others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168116996 | |||||
chr4:168116996
|
G | GACACACA others(9): Show |
121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(118): Show | 124 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.19-11074_19-11073i others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168116996 | |||||
chr4:168117019
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.19-11065G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117019 | ||||||
chr4:168117078
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-11006A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117078 | ||||||
chr4:168117199
|
C | G | 1 | a0002c0002t0001g0232 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.19-10885C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117199 | ||||||
chr4:168117457
|
C | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18952.hp1 NA18991.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-10627C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117457 | ||||||
chr4:168117650
|
A | G | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.19-10434A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117650 | ||||||
chr4:168117696
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19-10388A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117696 | ||||||
chr4:168117902
|
T | TACTC | 15 | a0001c0001t0001g0041a0001c0001t0001g0267a0001c0003t0001g0016others(12): Show | 15 | HG00099.hp1 HG01243.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.19-10149_19-10146d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117902 | |||||
chr4:168117902
|
TACTC | T | 14 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0237others(11): Show | 14 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.19-10149_19-10146d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117902 | |||||
chr4:168117931
|
ACTCACTC others(1): Show |
A | 11 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(8): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.19-10149_19-10142d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117931 | |||||
chr4:168117931
|
ACTCACTC others(5): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19-10149_19-10138d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117931 | |||||
chr4:168117935
|
A | ACTCACTC others(1): Show |
3 | a0001c0001t0001g0203a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.19-10146_19-10145i others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117935 | |||||
chr4:168117935
|
A | C | 6 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 7 | HG02280.hp1 HG02622.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-10149A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117935 | ||||||
chr4:168117935
|
ACTCC | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 38 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.19-10137_19-10134d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168117935 | |||||
chr4:168117939
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(114): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.19-10145C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117939 | ||||||
chr4:168117943
|
C | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(120): Show | 125 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.19-10141C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168117943 | ||||||
chr4:168118012
|
A | ATACAGGA others(1): Show |
118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(115): Show | 120 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19-10068_19-10061d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168118012 | |||||
chr4:168118096
|
T | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.19-9988T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168118096 | ||||||
chr4:168118210
|
GA | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0229others(10): Show | 15 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.19-9867delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168118210 | |||||
chr4:168118381
|
T | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.19-9703T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168118381 | ||||||
chr4:168118481
|
G | A | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19-9603G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168118481 | ||||||
chr4:168118777
|
C | T | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.19-9307C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168118777 | ||||||
chr4:168118810
|
A | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 16 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.19-9274A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168118810 | ||||||
chr4:168119191
|
G | A | 5 | a0001c0001t0001g0267a0001c0003t0001g0014a0001c0003t0001g0038others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-8893G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119191 | ||||||
chr4:168119235
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-8849A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119235 | ||||||
chr4:168119353
|
C | A | 1 | a0002c0002t0001g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.19-8731C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119353 | ||||||
chr4:168119355
|
A | G | 1 | a0002c0002t0001g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.19-8729A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119355 | ||||||
chr4:168119561
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19-8523G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119561 | ||||||
chr4:168119619
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-8465G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119619 | ||||||
chr4:168119624
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0237others(8): Show | 11 | HG01884.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-8460T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119624 | ||||||
chr4:168119964
|
C | A | 13 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(10): Show | 13 | HG00438.hp2 HG01361.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.19-8120C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168119964 | ||||||
chr4:168120028
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(172): Show | 180 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.19-8056A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120028 | ||||||
chr4:168120030
|
A | G | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.19-8054A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120030 | ||||||
chr4:168120382
|
C | T | 1 | a0002c0002t0001g0141 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.19-7702C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120382 | ||||||
chr4:168120539
|
TGTG | T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-7542_19-7540del others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168120539 | |||||
chr4:168120550
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(39): Show | 44 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.19-7534T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120550 | ||||||
chr4:168120585
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.19-7499G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120585 | ||||||
chr4:168120794
|
G | A | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-7290G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120794 | ||||||
chr4:168120849
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.19-7235C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168120849 | ||||||
chr4:168121016
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.19-7068A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121016 | ||||||
chr4:168121217
|
A | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0228 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.19-6867A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121217 | ||||||
chr4:168121217
|
AAC | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-6853_19-6852del others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168121217 | |||||
chr4:168121308
|
G | T | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-6776G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121308 | ||||||
chr4:168121432
|
A | C | 8 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273others(5): Show | 9 | HG01109.hp1 HG02280.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-6652A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121432 | ||||||
chr4:168121497
|
T | C | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | NA18960.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.19-6587T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121497 | ||||||
chr4:168121700
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.19-6384T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121700 | ||||||
chr4:168121701
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 175 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.19-6383G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121701 | ||||||
chr4:168121702
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-6382T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121702 | ||||||
chr4:168121920
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0002c0002t0001g0234 | 3 | HG01123.hp2 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.19-6164G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168121920 | ||||||
chr4:168122017
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0019others(109): Show | 114 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.19-6062delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168122017 | |||||
chr4:168122034
|
C | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 175 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.19-6050C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122034 | ||||||
chr4:168122039
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19-6045C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122039 | ||||||
chr4:168122298
|
G | A | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.19-5786G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122298 | ||||||
chr4:168122327
|
T | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(39): Show | 44 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.19-5757T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122327 | ||||||
chr4:168122484
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.19-5600T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122484 | ||||||
chr4:168122767
|
C | A | 3 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG02622.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.19-5317C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122767 | ||||||
chr4:168122840
|
C | T | 7 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-5244C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122840 | ||||||
chr4:168122857
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-5227A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168122857 | ||||||
chr4:168123027
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19-5057T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168123027 | ||||||
chr4:168123283
|
C | CA | 61 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(58): Show | 64 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.19-4793dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168123283 | |||||
chr4:168123283
|
C | CAA | 124 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0031others(121): Show | 125 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.19-4794_19-4793dup others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168123283 | |||||
chr4:168123743
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.19-4341T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168123743 | ||||||
chr4:168123797
|
A | T | 2 | a0002c0002t0001g0006a0002c0002t0001g0137 | 3 | HG01255.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.19-4287A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168123797 | ||||||
chr4:168124098
|
C | T | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-3986C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124098 | ||||||
chr4:168124135
|
C | T | 2 | a0001c0003t0001g0142a0002c0002t0001g0255 | 2 | HG01069.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.19-3949C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124135 | ||||||
chr4:168124161
|
C | T | 1 | a0001c0003t0001g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19-3923C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124161 | ||||||
chr4:168124463
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19-3621A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124463 | ||||||
chr4:168124589
|
C | A | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-3495C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124589 | ||||||
chr4:168124898
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-3186T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124898 | ||||||
chr4:168124980
|
G | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-3104G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124980 | ||||||
chr4:168124980
|
G | T | 6 | a0001c0001t0001g0267a0001c0003t0001g0014a0001c0003t0001g0038others(3): Show | 6 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-3104G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168124980 | ||||||
chr4:168125021
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.19-3063A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125021 | ||||||
chr4:168125163
|
A | T | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-2921A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125163 | ||||||
chr4:168125528
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-2556G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125528 | ||||||
chr4:168125557
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.19-2527G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125557 | ||||||
chr4:168125635
|
TAAA | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-2446_19-2444del others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168125635 | |||||
chr4:168125758
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.19-2326A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125758 | ||||||
chr4:168125955
|
T | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.19-2129T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168125955 | ||||||
chr4:168126052
|
A | G | 1 | a0001c0003t0001g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.19-2032A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126052 | ||||||
chr4:168126068
|
T | C | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0002c0002t0001g0115 | 3 | HG01123.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.19-2016T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126068 | ||||||
chr4:168126080
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(39): Show | 45 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(42): Show |
intron_variant | MODIFIER | c.19-2004C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126080 | ||||||
chr4:168126083
|
T | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(6): Show | 9 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.19-2001T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126083 | ||||||
chr4:168126110
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.19-1974A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126110 | ||||||
chr4:168126119
|
T | TA | 129 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0031others(126): Show | 130 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.19-1956dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168126119 | |||||
chr4:168126131
|
A | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.19-1953A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126131 | ||||||
chr4:168126153
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.19-1931T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126153 | ||||||
chr4:168126154
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0217a0001c0001t0001g0229others(6): Show | 11 | HG02280.hp1 HG02622.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.19-1930C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126154 | ||||||
chr4:168126177
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19-1907C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126177 | ||||||
chr4:168126586
|
G | A | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-1498G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126586 | ||||||
chr4:168126773
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.19-1311T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126773 | ||||||
chr4:168126950
|
A | G | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19-1134A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168126950 | ||||||
chr4:168127101
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.19-983T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127101 | ||||||
chr4:168127554
|
T | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0218others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.19-530T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127554 | ||||||
chr4:168127723
|
G | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-361G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127723 | ||||||
chr4:168127817
|
C | CT | 30 | a0001c0001t0001g0042a0001c0001t0001g0082a0001c0001t0001g0083others(27): Show | 30 | HG00438.hp1 HG00438.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.19-240dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTT | 20 | a0001c0001t0001g0041a0001c0001t0001g0095a0001c0001t0001g0117others(17): Show | 20 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.19-241_19-240dupTT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTT | 17 | a0001c0001t0001g0199a0001c0001t0001g0217a0001c0001t0001g0273others(14): Show | 18 | HG01106.hp2 HG01109.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.19-242_19-240dupTT others(1): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTT | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.19-245_19-240dupTT others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0229others(1): Show | 5 | HG01891.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-249_19-240dupTT others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0011t0001g0216others(2): Show | 5 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.19-250_19-240dupTT others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0218others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.19-251_19-240dupTT others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0227others(2): Show | 5 | HG02055.hp1 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-252_19-240dupTT others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0235a0001c0003t0001g0238 | 2 | HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.19-255_19-240dupTT others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
CT | C | 9 | a0001c0001t0001g0052a0001c0001t0001g0112a0001c0001t0001g0225others(6): Show | 9 | HG00140.hp1 HG01496.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-240delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127817
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.19-249_19-240delTT others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 168127817 | |||||
chr4:168127871
|
C | T | 5 | a0001c0001t0001g0267a0001c0003t0001g0014a0001c0003t0001g0038others(2): Show | 5 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.19-213C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127871 | ||||||
chr4:168127887
|
T | A | 1 | a0001c0001t0001g0066 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19-197T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127887 | ||||||
chr4:168127953
|
A | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.19-131A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127953 | ||||||
chr4:168127955
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.19-129T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168127955 | ||||||
chr4:168128004
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.19-80A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168128004 | ||||||
chr4:168128036
|
C | T | 3 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124 | 3 | HG01891.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.19-48C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 1/11 | chr4 | 168128036 | ||||||
chr4:168128214
|
T | A | 1 | a0001c0001t0001g0067 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.100+49T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128214 | ||||||
chr4:168128255
|
T | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+90T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128255 | ||||||
chr4:168128284
|
C | CA | 12 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0272others(9): Show | 13 | HG00140.hp2 HG01891.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+133dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 168128284 | |||||
chr4:168128284
|
CA | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+133delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 168128284 | |||||
chr4:168128317
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.100+152T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128317 | ||||||
chr4:168128446
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(118): Show | 122 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.100+281A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128446 | ||||||
chr4:168128621
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(91): Show | 95 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.100+456G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128621 | ||||||
chr4:168128704
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(118): Show | 122 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.100+539C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128704 | ||||||
chr4:168128737
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02451.hp2 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+572G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128737 | ||||||
chr4:168128775
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.100+610C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128775 | ||||||
chr4:168128782
|
C | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+617C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128782 | ||||||
chr4:168128903
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0229others(4): Show | 8 | HG02258.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+738G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128903 | ||||||
chr4:168128984
|
A | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100+819A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168128984 | ||||||
chr4:168129100
|
A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.100+935A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168129100 | ||||||
chr4:168130062
|
G | A | 5 | a0002c0002t0001g0136a0002c0002t0001g0150a0002c0002t0001g0151others(2): Show | 5 | HG00621.hp1 HG01099.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+1897G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168130062 | ||||||
chr4:168130076
|
T | C | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0238 | 3 | HG02258.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.100+1911T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168130076 | ||||||
chr4:168130885
|
T | C | 1 | a0002c0002t0001g0133 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.100+2720T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168130885 | ||||||
chr4:168131106
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+2941T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168131106 | ||||||
chr4:168131206
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG01361.hp1 HG02451.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+3041C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168131206 | ||||||
chr4:168131386
|
A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.100+3221A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168131386 | ||||||
chr4:168131696
|
G | A | 7 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG00639.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+3531G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168131696 | ||||||
chr4:168131956
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 25 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.100+3791C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168131956 | ||||||
chr4:168132517
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+4352A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168132517 | ||||||
chr4:168132636
|
G | A | 1 | a0001c0003t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.100+4471G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168132636 | ||||||
chr4:168132774
|
T | A | 2 | a0001c0008t0001g0247a0001c0008t0001g0248 | 2 | NA18939.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.100+4609T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168132774 | ||||||
chr4:168132779
|
G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.100+4614G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168132779 | ||||||
chr4:168132973
|
T | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0218others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+4808T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168132973 | ||||||
chr4:168133029
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+4864A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133029 | ||||||
chr4:168133065
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100+4900T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133065 | ||||||
chr4:168133194
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 13 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.100+5029G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133194 | ||||||
chr4:168133294
|
T | A | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100+5129T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133294 | ||||||
chr4:168133294
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100+5129T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133294 | ||||||
chr4:168133319
|
A | T | 6 | a0001c0011t0001g0216a0003c0004t0001g0096a0003c0004t0001g0220others(3): Show | 6 | HG02055.hp2 HG02717.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+5154A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133319 | ||||||
chr4:168133429
|
G | T | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+5264G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133429 | ||||||
chr4:168133809
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100+5644C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168133809 | ||||||
chr4:168133962
|
G | GA | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(43): Show | 49 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.101-5522dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 168133962 | |||||
chr4:168134015
|
A | C | 28 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0273others(25): Show | 28 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.101-5471A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134015 | ||||||
chr4:168134034
|
T | C | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.101-5452T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134034 | ||||||
chr4:168134257
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.101-5229T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134257 | ||||||
chr4:168134360
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101-5126T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134360 | ||||||
chr4:168134620
|
G | T | 1 | a0002c0002t0001g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101-4866G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134620 | ||||||
chr4:168134751
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.101-4735T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134751 | ||||||
chr4:168134793
|
C | T | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.101-4693C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134793 | ||||||
chr4:168134825
|
T | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0117others(12): Show | 17 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-4661T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134825 | ||||||
chr4:168134886
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.101-4600T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134886 | ||||||
chr4:168134943
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.101-4543A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168134943 | ||||||
chr4:168135195
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.101-4291G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135195 | ||||||
chr4:168135211
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.101-4275A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135211 | ||||||
chr4:168135260
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.101-4226A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135260 | ||||||
chr4:168135303
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(28): Show | 32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-4183T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135303 | ||||||
chr4:168135365
|
A | T | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-4121A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135365 | ||||||
chr4:168135472
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0199a0002c0002t0001g0115 | 3 | HG01123.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.101-4014A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135472 | ||||||
chr4:168135626
|
C | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.101-3860C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135626 | ||||||
chr4:168135896
|
T | A | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | NA18960.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.101-3590T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135896 | ||||||
chr4:168135983
|
G | A | 1 | a0002c0002t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.101-3503G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168135983 | ||||||
chr4:168136090
|
C | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101-3396C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136090 | ||||||
chr4:168136120
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0117others(12): Show | 17 | HG02258.hp2 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-3366G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136120 | ||||||
chr4:168136148
|
C | T | 2 | a0001c0001t0001g0217a0002c0002t0001g0232 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-3338C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136148 | ||||||
chr4:168136157
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0036 | 3 | HG01081.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.101-3329C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136157 | ||||||
chr4:168136534
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.101-2952T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136534 | ||||||
chr4:168136854
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.101-2632T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168136854 | ||||||
chr4:168137084
|
T | A | 1 | a0002c0002t0001g0091 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.101-2402T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137084 | ||||||
chr4:168137090
|
G | C | 4 | a0001c0003t0001g0022a0001c0003t0001g0028a0001c0003t0001g0032others(1): Show | 4 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-2396G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137090 | ||||||
chr4:168137110
|
G | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.101-2376G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137110 | ||||||
chr4:168137153
|
G | T | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-2333G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137153 | ||||||
chr4:168137179
|
A | T | 1 | a0001c0003t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.101-2307A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137179 | ||||||
chr4:168137270
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.101-2216T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137270 | ||||||
chr4:168137480
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0227others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-2006G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137480 | ||||||
chr4:168137527
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.101-1959T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137527 | ||||||
chr4:168137670
|
T | C | 3 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124 | 3 | HG01891.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.101-1816T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137670 | ||||||
chr4:168137747
|
T | C | 1 | a0002c0002t0001g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-1739T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137747 | ||||||
chr4:168137828
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 167 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.101-1658A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137828 | ||||||
chr4:168137831
|
G | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.101-1655G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137831 | ||||||
chr4:168137912
|
T | C | 28 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0273others(25): Show | 28 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.101-1574T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168137912 | ||||||
chr4:168137959
|
CT | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0117others(16): Show | 21 | HG00099.hp1 HG01361.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.101-1510delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 168137959 | |||||
chr4:168138023
|
G | A | 1 | a0002c0002t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-1463G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138023 | ||||||
chr4:168138389
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.101-1097T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138389 | ||||||
chr4:168138396
|
GA | G | 10 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(7): Show | 10 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-1080delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 168138396 | |||||
chr4:168138703
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-783T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138703 | ||||||
chr4:168138749
|
T | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.101-737T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138749 | ||||||
chr4:168138760
|
T | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(91): Show | 95 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.101-726T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138760 | ||||||
chr4:168138846
|
A | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(173): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.101-640A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138846 | ||||||
chr4:168138892
|
C | A | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.101-594C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138892 | ||||||
chr4:168138935
|
G | A | 2 | a0001c0001t0001g0039a0002c0002t0001g0040 | 2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.101-551G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168138935 | ||||||
chr4:168139013
|
T | C | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.101-473T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139013 | ||||||
chr4:168139072
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.101-414A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139072 | ||||||
chr4:168139081
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(120): Show | 124 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.101-405T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139081 | ||||||
chr4:168139095
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.101-391C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139095 | ||||||
chr4:168139158
|
A | G | 1 | a0002c0002t0001g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.101-328A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139158 | ||||||
chr4:168139206
|
G | C | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-280G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139206 | ||||||
chr4:168139397
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.101-89G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 2/11 | chr4 | 168139397 | ||||||
chr4:168139694
|
T | C | 1 | a0001c0003t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+114T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168139694 | ||||||
chr4:168139938
|
A | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 26 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.195+358A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168139938 | ||||||
chr4:168140254
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0117others(7): Show | 11 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+674A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140254 | ||||||
chr4:168140276
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(119): Show | 123 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.195+696A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140276 | ||||||
chr4:168140325
|
T | G | 1 | a0003c0004t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.195+745T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140325 | ||||||
chr4:168140608
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195+1028T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140608 | ||||||
chr4:168140618
|
C | CT | 27 | a0001c0001t0001g0267a0001c0001t0001g0272a0001c0001t0001g0273others(24): Show | 27 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.195+1051dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168140618 | |||||
chr4:168140618
|
CT | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0017others(26): Show | 32 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.195+1051delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168140618 | |||||
chr4:168140649
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG01123.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.195+1069G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140649 | ||||||
chr4:168140767
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+1187C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168140767 | ||||||
chr4:168141146
|
A | G | 94 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(91): Show | 95 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.195+1566A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141146 | ||||||
chr4:168141257
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.195+1677C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141257 | ||||||
chr4:168141378
|
T | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0042others(91): Show | 95 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.195+1798T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141378 | ||||||
chr4:168141656
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.195+2076G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141656 | ||||||
chr4:168141818
|
C | G | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.195+2238C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141818 | ||||||
chr4:168141901
|
C | T | 5 | a0001c0001t0001g0278a0002c0002t0001g0006a0002c0002t0001g0234others(2): Show | 6 | HG02280.hp1 HG02965.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+2321C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141901 | ||||||
chr4:168141958
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0055others(1): Show | 5 | HG01106.hp1 HG01261.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+2378A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141958 | ||||||
chr4:168141968
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195+2388T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168141968 | ||||||
chr4:168142101
|
G | A | 1 | a0002c0002t0001g0145 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.195+2521G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142101 | ||||||
chr4:168142232
|
A | G | 2 | a0001c0001t0001g0217a0002c0002t0001g0232 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.195+2652A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142232 | ||||||
chr4:168142405
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.195+2825A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142405 | ||||||
chr4:168142484
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195+2904T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142484 | ||||||
chr4:168142516
|
C | T | 1 | a0001c0001t0001g0253 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.195+2936C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142516 | ||||||
chr4:168142783
|
C | T | 2 | a0001c0003t0001g0029a0001c0003t0001g0030 | 2 | NA18943.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.195+3203C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168142783 | ||||||
chr4:168143101
|
A | C | 1 | a0001c0003t0001g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+3521A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143101 | ||||||
chr4:168143165
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195+3585C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143165 | ||||||
chr4:168143294
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.195+3714T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143294 | ||||||
chr4:168143366
|
G | A | 1 | a0001c0003t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+3786G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143366 | ||||||
chr4:168143626
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.195+4046G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143626 | ||||||
chr4:168143721
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+4141G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143721 | ||||||
chr4:168143971
|
A | C | 1 | a0002c0002t0001g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.195+4391A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168143971 | ||||||
chr4:168144343
|
C | T | 1 | a0001c0003t0001g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.195+4763C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144343 | ||||||
chr4:168144354
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.195+4774T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144354 | ||||||
chr4:168144366
|
T | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0271a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+4786T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144366 | ||||||
chr4:168144409
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.195+4829A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144409 | ||||||
chr4:168144598
|
G | T | 1 | a0001c0003t0001g0022 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.195+5018G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144598 | ||||||
chr4:168144655
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.195+5075A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168144655 | ||||||
chr4:168145114
|
G | A | 1 | a0001c0003t0001g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.195+5534G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145114 | ||||||
chr4:168145117
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.195+5537C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145117 | ||||||
chr4:168145394
|
G | A | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+5814G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145394 | ||||||
chr4:168145476
|
G | A | 3 | a0002c0002t0001g0006a0002c0002t0001g0274a0002c0002t0001g0275 | 4 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+5896G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145476 | ||||||
chr4:168145476
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.195+5896G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145476 | ||||||
chr4:168145538
|
G | T | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.195+5958G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145538 | ||||||
chr4:168145712
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.195+6132T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145712 | ||||||
chr4:168145775
|
C | G | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195+6195C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145775 | ||||||
chr4:168145904
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0229a0001c0001t0001g0235others(2): Show | 6 | HG02258.hp1 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+6324T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168145904 | ||||||
chr4:168145925
|
CT | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.195+6356delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168145925 | |||||
chr4:168146034
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.195+6454G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146034 | ||||||
chr4:168146174
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0271a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+6594G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146174 | ||||||
chr4:168146228
|
A | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00639.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.195+6648A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146228 | ||||||
chr4:168146314
|
A | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0117others(7): Show | 11 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.195+6734A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146314 | ||||||
chr4:168146387
|
C | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.195+6807C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146387 | ||||||
chr4:168146697
|
G | A | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0218others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.195+7117G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168146697 | ||||||
chr4:168146759
|
C | CA | 7 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+7180dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168146759 | |||||
chr4:168147025
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.195+7445C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147025 | ||||||
chr4:168147177
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.195+7597T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147177 | ||||||
chr4:168147546
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.195+7966C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147546 | ||||||
chr4:168147669
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.195+8089T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147669 | ||||||
chr4:168147676
|
C | T | 1 | a0001c0003t0001g0013 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.195+8096C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147676 | ||||||
chr4:168147790
|
C | T | 3 | a0001c0009t0001g0207a0001c0009t0001g0208a0002c0012t0001g0113 | 3 | HG00099.hp1 HG01361.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.195+8210C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147790 | ||||||
chr4:168147954
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0271a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG03041.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+8374C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168147954 | ||||||
chr4:168148023
|
A | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.195+8443A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148023 | ||||||
chr4:168148173
|
A | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.195+8593A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148173 | ||||||
chr4:168148174
|
A | AT | 6 | a0001c0001t0001g0198a0001c0001t0001g0199a0002c0002t0001g0006others(3): Show | 7 | HG01123.hp2 HG02280.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.195+8610dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168148174 | |||||
chr4:168148174
|
AT | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0017others(88): Show | 93 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.195+8610delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168148174 | |||||
chr4:168148356
|
G | A | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(106): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.195+8776G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148356 | ||||||
chr4:168148411
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.195+8831C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148411 | ||||||
chr4:168148412
|
G | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0271 | 2 | NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.195+8832G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148412 | ||||||
chr4:168148418
|
G | A | 1 | a0002c0002t0001g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.195+8838G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148418 | ||||||
chr4:168148445
|
A | G | 40 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(37): Show | 41 | HG00323.hp1 HG00639.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.195+8865A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148445 | ||||||
chr4:168148460
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.195+8880T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148460 | ||||||
chr4:168148509
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.195+8929C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148509 | ||||||
chr4:168148599
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.195+9019A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148599 | ||||||
chr4:168148669
|
T | C | 1 | a0002c0002t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.195+9089T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148669 | ||||||
chr4:168148672
|
T | C | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.195+9092T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148672 | ||||||
chr4:168148680
|
A | C | 2 | a0001c0001t0001g0217a0002c0002t0001g0232 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.195+9100A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148680 | ||||||
chr4:168148949
|
T | C | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+9369T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168148949 | ||||||
chr4:168149006
|
C | T | 6 | a0002c0002t0001g0115a0003c0004t0001g0096a0003c0004t0001g0220others(3): Show | 6 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+9426C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149006 | ||||||
chr4:168149130
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG00639.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.195+9550G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149130 | ||||||
chr4:168149139
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.195+9559A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149139 | ||||||
chr4:168149245
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.195+9665T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149245 | ||||||
chr4:168149273
|
C | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0273 | 2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.195+9693C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149273 | ||||||
chr4:168149620
|
T | C | 4 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0257others(1): Show | 4 | HG01361.hp1 HG01515.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+10040T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149620 | ||||||
chr4:168149723
|
T | C | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.195+10143T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149723 | ||||||
chr4:168149831
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.195+10251G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149831 | ||||||
chr4:168149883
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0055others(2): Show | 6 | HG00738.hp1 HG01106.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+10303C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149883 | ||||||
chr4:168149895
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.195+10315G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149895 | ||||||
chr4:168149997
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.195+10417C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149997 | ||||||
chr4:168149997
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0071 | 2 | NA18942.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.195+10417C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168149997 | ||||||
chr4:168150247
|
G | A | 2 | a0001c0001t0001g0217a0002c0002t0001g0232 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.195+10667G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150247 | ||||||
chr4:168150253
|
AG | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0218others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.195+10674delG | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150253 | ||||||
chr4:168150318
|
T | A | 1 | a0002c0002t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.195+10738T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150318 | ||||||
chr4:168150321
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | HG02622.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.195+10741G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150321 | ||||||
chr4:168150493
|
C | T | 4 | a0002c0002t0001g0006a0002c0002t0001g0226a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.195+10913C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150493 | ||||||
chr4:168150651
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0211others(4): Show | 8 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.195+11071C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150651 | ||||||
chr4:168150724
|
G | A | 3 | a0002c0002t0001g0156a0002c0002t0001g0183a0002c0002t0001g0206 | 3 | NA18971.hp2 NA19058.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.195+11144G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150724 | ||||||
chr4:168150782
|
T | C | 2 | a0002c0002t0001g0157a0002c0002t0001g0190 | 2 | HG02165.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.195+11202T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150782 | ||||||
chr4:168150808
|
A | C | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 30 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.195+11228A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150808 | ||||||
chr4:168150811
|
C | T | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 30 | HG00099.hp2 HG00735.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.195+11231C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168150811 | ||||||
chr4:168151005
|
C | T | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+11425C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151005 | ||||||
chr4:168151322
|
T | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-11206T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151322 | ||||||
chr4:168151379
|
A | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-11149A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151379 | ||||||
chr4:168151422
|
G | A | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-11106G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151422 | ||||||
chr4:168151603
|
C | T | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.196-10925C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151603 | ||||||
chr4:168151632
|
G | GTA | 12 | a0001c0001t0001g0117a0001c0001t0001g0217a0001c0001t0001g0218others(9): Show | 13 | HG01884.hp1 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-10885_196-1088 others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168151632 | |||||
chr4:168151737
|
G | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(182): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.196-10791G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168151737 | ||||||
chr4:168152033
|
T | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196-10495T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152033 | ||||||
chr4:168152167
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-10361A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152167 | ||||||
chr4:168152192
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(47): Show | 51 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.196-10336G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152192 | ||||||
chr4:168152262
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.196-10266A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152262 | ||||||
chr4:168152393
|
G | T | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-10135G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152393 | ||||||
chr4:168152586
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-9942G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152586 | ||||||
chr4:168152869
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-9659G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152869 | ||||||
chr4:168152935
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-9593A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152935 | ||||||
chr4:168152952
|
T | A | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196-9576T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168152952 | ||||||
chr4:168153058
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(274): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.196-9470A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153058 | ||||||
chr4:168153211
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-9317T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153211 | ||||||
chr4:168153410
|
A | G | 1 | a0002c0002t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.196-9118A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153410 | ||||||
chr4:168153422
|
C | CA | 14 | a0002c0002t0001g0040a0002c0002t0001g0072a0002c0002t0001g0075others(11): Show | 14 | HG00423.hp2 HG01255.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-9087dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153422 | |||||
chr4:168153422
|
CAA | C | 17 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0228others(14): Show | 18 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.196-9088_196-9087d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153422 | |||||
chr4:168153422
|
CAAA | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(23): Show | 26 | HG01496.hp2 HG01891.hp1 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.196-9089_196-9087d others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153422 | |||||
chr4:168153423
|
AAAAAAAA others(29): Show |
A | 34 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(31): Show | 35 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.196-9093_196-9058d others(38): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153423 | |||||
chr4:168153424
|
AAAAAAAA others(28): Show |
A | 6 | a0001c0003t0001g0014a0003c0004t0001g0096a0003c0004t0001g0220others(3): Show | 6 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-9092_196-9058d others(37): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153424 | |||||
chr4:168153428
|
AAAAAAAA others(24): Show |
A | 28 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(25): Show | 29 | HG00738.hp1 HG01081.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-9088_196-9058d others(33): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153428 | |||||
chr4:168153429
|
AAAAAAAA others(23): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196-9087_196-9058d others(32): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153429 | |||||
chr4:168153430
|
A | C | 16 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(13): Show | 16 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.196-9098A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153430 | ||||||
chr4:168153432
|
A | C | 1 | a0002c0002t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.196-9096A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153432 | ||||||
chr4:168153434
|
AAAAAAAA others(18): Show |
A | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-9086_196-9062d others(27): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153434 | |||||
chr4:168153436
|
A | C | 20 | a0002c0002t0001g0006a0002c0002t0001g0081a0002c0002t0001g0143others(17): Show | 21 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.196-9092A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153436 | ||||||
chr4:168153436
|
AAAAAACA others(16): Show |
A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-9086_196-9064d others(25): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153436 | |||||
chr4:168153437
|
A | C | 1 | a0002c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196-9091A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153437 | ||||||
chr4:168153437
|
AAAAACAA others(4): Show |
A | 19 | a0001c0001t0001g0008a0001c0001t0001g0079a0001c0001t0001g0080others(16): Show | 19 | HG00438.hp2 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.196-9086_196-9076d others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153437 | |||||
chr4:168153438
|
AAAACAAA others(3): Show |
A | 17 | a0001c0001t0001g0019a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 17 | HG00735.hp1 HG01109.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-9086_196-9077d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153438 | |||||
chr4:168153439
|
AAACAAAA others(2): Show |
A | 13 | a0001c0001t0001g0073a0001c0001t0001g0076a0001c0001t0001g0077others(10): Show | 13 | HG00639.hp1 HG00738.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-9086_196-9078d others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153439 | |||||
chr4:168153440
|
AACAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0082a0001c0001t0001g0098a0001c0001t0001g0100others(4): Show | 7 | HG00140.hp1 HG01099.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-9086_196-9079d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153440 | |||||
chr4:168153441
|
ACAAAAAC others(6): Show |
A | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196-9086_196-9074d others(15): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153441 | ||||||
chr4:168153442
|
C | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0097a0001c0001t0001g0210others(4): Show | 8 | HG00099.hp1 HG01109.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-9086C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153442 | ||||||
chr4:168153447
|
ACAAAAAC others(5): Show |
A | 6 | a0001c0001t0001g0004a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 7 | HG00099.hp1 HG01109.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-9080_196-9069d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153447 | ||||||
chr4:168153448
|
C | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG02451.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-9080C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153448 | ||||||
chr4:168153454
|
C | A | 61 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0057others(58): Show | 61 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.196-9074C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153454 | ||||||
chr4:168153459
|
C | A | 62 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0041others(59): Show | 62 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.196-9069C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153459 | ||||||
chr4:168153459
|
C | CA | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-9058dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153459 | |||||
chr4:168153459
|
CA | C | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-9058delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153459 | |||||
chr4:168153461
|
A | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-9067A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153461 | ||||||
chr4:168153464
|
A | C | 1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-9064A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153464 | ||||||
chr4:168153467
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.196-9061A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153467 | ||||||
chr4:168153493
|
A | ACAG | 98 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(95): Show | 100 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.196-9034_196-9032d others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153493 | |||||
chr4:168153736
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196-8792C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153736 | ||||||
chr4:168153821
|
T | A | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-8707T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153821 | ||||||
chr4:168153839
|
T | C | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8689T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153839 | ||||||
chr4:168153981
|
T | C | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-8547T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168153981 | ||||||
chr4:168153981
|
T | TAC | 5 | a0001c0001t0001g0017a0002c0002t0001g0132a0002c0002t0001g0133others(2): Show | 5 | HG00423.hp2 HG01074.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-8526_196-8525d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153981 | |||||
chr4:168153981
|
T | TACAC | 10 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 11 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-8528_196-8525d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153981 | |||||
chr4:168153981
|
T | TACACACA others(5): Show |
3 | a0002c0002t0001g0270a0006c0007t0001g0015a0006c0007t0001g0268 | 3 | HG00639.hp2 HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.196-8536_196-8525d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153981 | |||||
chr4:168153981
|
TAC | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 132 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.196-8526_196-8525d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153981 | |||||
chr4:168153981
|
TACAC | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0073a0001c0001t0001g0092others(1): Show | 4 | HG01515.hp2 NA18939.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-8528_196-8525d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153981 | |||||
chr4:168153998
|
A | ACACACAC others(6): Show |
1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196-8525_196-8524i others(15): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168153998 | |||||
chr4:168154000
|
A | ACG | 14 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0153others(11): Show | 14 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-8527_196-8526i others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168154000 | |||||
chr4:168154012
|
G | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-8516G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154012 | ||||||
chr4:168154023
|
T | C | 1 | a0004c0005t0001g0049 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.196-8505T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154023 | ||||||
chr4:168154040
|
C | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-8488C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154040 | ||||||
chr4:168154405
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-8123G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154405 | ||||||
chr4:168154482
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.196-8046G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154482 | ||||||
chr4:168154523
|
G | A | 2 | a0002c0002t0001g0132a0002c0002t0001g0185 | 2 | HG00423.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.196-8005G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154523 | ||||||
chr4:168154623
|
T | C | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7905T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154623 | ||||||
chr4:168154656
|
G | A | 1 | a0002c0002t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.196-7872G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154656 | ||||||
chr4:168154709
|
G | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196-7819G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154709 | ||||||
chr4:168154762
|
T | C | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-7766T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154762 | ||||||
chr4:168154936
|
G | A | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7592G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168154936 | ||||||
chr4:168155041
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.196-7487A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155041 | ||||||
chr4:168155119
|
ATTAT | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 24 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.196-7403_196-7400d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155119 | |||||
chr4:168155356
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196-7172A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155356 | ||||||
chr4:168155380
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.196-7148A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155380 | ||||||
chr4:168155397
|
T | TTA | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.196-7125_196-7124d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155397 | |||||
chr4:168155428
|
TA | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-7098delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155428 | |||||
chr4:168155444
|
T | TAAATTAT others(32): Show |
2 | a0002c0002t0001g0081a0002c0002t0001g0182 | 2 | HG01952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.196-7084_196-7083i others(41): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155444 | ||||||
chr4:168155444
|
TGAATTAT others(44): Show |
T | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-7083_196-7033d others(53): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155444 | ||||||
chr4:168155444
|
TGAATTAT others(81): Show |
T | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-7083_196-6996d others(90): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155444 | ||||||
chr4:168155445
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(68): Show | 74 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.196-7083G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155445 | ||||||
chr4:168155445
|
G | T | 2 | a0002c0002t0001g0081a0002c0002t0001g0182 | 2 | HG01952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.196-7083G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155445 | ||||||
chr4:168155457
|
T | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 57 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.196-7071T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155457 | ||||||
chr4:168155457
|
T | TTATAATA others(22): Show |
4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-7053_196-7025d others(31): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155457 | |||||
chr4:168155460
|
T | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 57 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.196-7068T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155460 | ||||||
chr4:168155461
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-7067A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155461 | ||||||
chr4:168155468
|
A | AATTATAT others(142): Show |
13 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(10): Show | 13 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-7054_196-7053i others(151): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155468 | |||||
chr4:168155468
|
AATTATAA others(7): Show |
A | 10 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(7): Show | 11 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-7053_196-7040d others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155468 | |||||
chr4:168155474
|
A | ATAATATA others(1): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-7054_196-7053i others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155474 | ||||||
chr4:168155475
|
A | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(28): Show | 32 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.196-7053A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155475 | ||||||
chr4:168155477
|
T | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(41): Show | 45 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.196-7051T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155477 | ||||||
chr4:168155482
|
T | TA | 13 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(10): Show | 13 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-7045dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155482
|
T | TAATTATA others(55): Show |
30 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(27): Show | 31 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.196-7045_196-7044i others(64): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155482
|
T | TAATTATA others(93): Show |
1 | a0001c0003t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.196-7045_196-7044i others(102): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155482
|
T | TATTATAA others(9): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-7040_196-7039i others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155482
|
T | TATTATAT others(30): Show |
2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | NA18962.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.196-6978_196-6942d others(39): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155482
|
TATTATAT others(30): Show |
T | 1 | a0002c0002t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.196-6978_196-6942d others(39): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155482 | |||||
chr4:168155486
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-7042A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155486 | ||||||
chr4:168155496
|
T | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(15): Show | 18 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-7032T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155496 | ||||||
chr4:168155504
|
T | A | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-7024T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155504 | ||||||
chr4:168155510
|
AAAATATA others(1): Show |
A | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-7015_196-7008d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155510 | |||||
chr4:168155511
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-7017A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155511 | ||||||
chr4:168155512
|
A | AT | 67 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 70 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.196-7016_196-7015i others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155512 | ||||||
chr4:168155513
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-7015A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155513 | ||||||
chr4:168155519
|
A | AATATATA others(43): Show |
1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-7007_196-7006i others(52): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155519 | |||||
chr4:168155519
|
A | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-7009A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155519 | ||||||
chr4:168155533
|
T | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-6995T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155533 | ||||||
chr4:168155545
|
A | T | 1 | a0002c0002t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196-6983A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155545 | ||||||
chr4:168155549
|
A | AATATATA others(106): Show |
1 | a0002c0002t0001g0081 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.196-6942_196-6941i others(115): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155549 | |||||
chr4:168155549
|
A | AATATATA others(105): Show |
1 | a0002c0002t0001g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.196-6942_196-6941i others(114): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155549 | |||||
chr4:168155549
|
A | AATATATA others(31): Show |
3 | a0002c0002t0001g0159a0002c0002t0001g0160a0002c0002t0001g0161 | 3 | HG02145.hp1 NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.196-6925_196-6888d others(40): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155549 | |||||
chr4:168155549
|
A | AT | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 88 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-6979_196-6978i others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155549 | ||||||
chr4:168155565
|
A | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-6963A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155565 | ||||||
chr4:168155602
|
A | AATATATA others(26): Show |
1 | a0002c0002t0001g0269 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.196-6912_196-6880d others(35): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155602 | |||||
chr4:168155621
|
T | C | 1 | a0001c0009t0001g0207 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.196-6907T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155621 | ||||||
chr4:168155624
|
ATATATAT others(3): Show |
A | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6889_196-6880d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155624 | |||||
chr4:168155635
|
T | TATATA | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6892_196-6888d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155635 | |||||
chr4:168155649
|
C | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6879C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155649 | ||||||
chr4:168155655
|
A | AAATATAT others(2): Show |
3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6873_196-6872i others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155655 | ||||||
chr4:168155656
|
T | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6872T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155656 | ||||||
chr4:168155658
|
G | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6870G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155658 | ||||||
chr4:168155664
|
T | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6864T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155664 | ||||||
chr4:168155685
|
A | AATATATA others(9): Show |
1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6842_196-6841i others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155685 | |||||
chr4:168155692
|
T | C | 8 | a0002c0002t0001g0138a0002c0002t0001g0150a0002c0002t0001g0151others(5): Show | 8 | HG00621.hp1 HG00741.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6836T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155692 | ||||||
chr4:168155705
|
A | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6823A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155705 | ||||||
chr4:168155707
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.196-6821A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155707 | ||||||
chr4:168155712
|
A | T | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6816A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155712 | ||||||
chr4:168155712
|
ATAT | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.196-6812_196-6810d others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155712 | |||||
chr4:168155713
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6815T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155713 | ||||||
chr4:168155721
|
A | ATAAATAT others(2): Show |
3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6807_196-6806i others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155721 | ||||||
chr4:168155721
|
A | ATAATT | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6807_196-6806i others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155721 | ||||||
chr4:168155721
|
AATATAAT others(26): Show |
A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-6768_196-6736d others(35): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155721 | |||||
chr4:168155725
|
T | C | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6803T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155725 | ||||||
chr4:168155726
|
A | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6802A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155726 | ||||||
chr4:168155727
|
A | T | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6801A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155727 | ||||||
chr4:168155729
|
ATATGATA others(43): Show |
A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-6795_196-6746d others(52): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155729 | |||||
chr4:168155730
|
T | C | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-6798T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155730 | ||||||
chr4:168155732
|
T | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6796T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155732 | ||||||
chr4:168155733
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6795G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155733 | ||||||
chr4:168155733
|
G | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.196-6795G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155733 | ||||||
chr4:168155734
|
A | G | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6794A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155734 | ||||||
chr4:168155740
|
C | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6788C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155740 | ||||||
chr4:168155740
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6788C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155740 | ||||||
chr4:168155747
|
T | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(134): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.196-6781T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155747 | ||||||
chr4:168155753
|
T | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6775T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155753 | ||||||
chr4:168155754
|
T | A | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6774T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155754 | ||||||
chr4:168155754
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(1): Show | 5 | HG01123.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6774T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155754 | ||||||
chr4:168155755
|
A | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6773A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155755 | ||||||
chr4:168155758
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6770T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155758 | ||||||
chr4:168155759
|
A | AATATATG others(77): Show |
12 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0153others(9): Show | 12 | HG01496.hp2 HG01943.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.196-6749_196-6748i others(86): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155759 | |||||
chr4:168155759
|
A | AATATATG others(77): Show |
1 | a0002c0002t0001g0146 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196-6756_196-6755i others(86): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155759 | |||||
chr4:168155766
|
G | A | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0014 | 3 | HG02258.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6762G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155766 | ||||||
chr4:168155766
|
G | C | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6762G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155766 | ||||||
chr4:168155766
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(152): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.196-6762G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155766 | ||||||
chr4:168155773
|
C | G | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6755C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155773 | ||||||
chr4:168155773
|
C | T | 2 | a0001c0001t0001g0129a0001c0003t0001g0014 | 2 | HG00735.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6755C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155773 | ||||||
chr4:168155773
|
CATATATT | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 102 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.196-6741_196-6735d others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155773 | |||||
chr4:168155773
|
CATATATT others(21): Show |
C | 1 | a0002c0002t0001g0177 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.196-6748_196-6721d others(30): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155773 | |||||
chr4:168155777
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6751T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155777 | ||||||
chr4:168155780
|
T | C | 4 | a0002c0002t0001g0044a0002c0002t0001g0108a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6748T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155780 | ||||||
chr4:168155780
|
T | G | 50 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0129others(47): Show | 51 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.196-6748T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155780 | ||||||
chr4:168155780
|
T | TATATATT others(5): Show |
1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6747_196-6736d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155780 | |||||
chr4:168155784
|
TATTATAT others(4): Show |
T | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6743_196-6733d others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155784 | ||||||
chr4:168155785
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.196-6743A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155785 | ||||||
chr4:168155786
|
TTA | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.196-6735_196-6734d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155786 | |||||
chr4:168155786
|
TTATATAT others(2): Show |
T | 3 | a0001c0001t0001g0219a0001c0003t0001g0032a0001c0003t0001g0142 | 3 | HG01069.hp1 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.196-6735_196-6727d others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155786 | |||||
chr4:168155787
|
T | A | 4 | a0001c0003t0001g0014a0002c0002t0001g0270a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6741T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155787 | ||||||
chr4:168155787
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6741T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155787 | ||||||
chr4:168155787
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 148 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.196-6741T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155787 | ||||||
chr4:168155792
|
A | G | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6736A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155792 | ||||||
chr4:168155794
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6734A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155794 | ||||||
chr4:168155794
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.196-6734A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155794 | ||||||
chr4:168155794
|
A | T | 6 | a0001c0001t0001g0217a0001c0003t0001g0014a0002c0002t0001g0040others(3): Show | 6 | HG02647.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-6734A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155794 | ||||||
chr4:168155801
|
A | C | 19 | a0001c0001t0001g0217a0001c0001t0001g0235a0001c0001t0001g0236others(16): Show | 19 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-6727A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155801 | ||||||
chr4:168155801
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0117others(27): Show | 31 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.196-6727A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155801 | ||||||
chr4:168155801
|
A | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0098others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.196-6727A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155801 | ||||||
chr4:168155808
|
G | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(39): Show | 43 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.196-6720G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155808 | ||||||
chr4:168155808
|
G | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 26 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.196-6720G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155808 | ||||||
chr4:168155809
|
A | C | 1 | a0001c0003t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-6719A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155809 | ||||||
chr4:168155815
|
T | A | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-6713T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155815 | ||||||
chr4:168155815
|
T | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-6713T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155815 | ||||||
chr4:168155815
|
T | G | 47 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(44): Show | 48 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.196-6713T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155815 | ||||||
chr4:168155815
|
T | TATATTAT others(78): Show |
1 | a0002c0002t0001g0197 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.196-6709_196-6708i others(87): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155815 | |||||
chr4:168155820
|
ATG | A | 3 | a0001c0001t0001g0217a0001c0003t0001g0014a0002c0002t0001g0115 | 3 | NA19030.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6707_196-6706d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155820 | ||||||
chr4:168155821
|
TGATATAT others(28): Show |
T | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6706_196-6672d others(37): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155821 | ||||||
chr4:168155822
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-6706G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155822 | ||||||
chr4:168155822
|
G | C | 3 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0250 | 3 | HG02258.hp1 HG02970.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.196-6706G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155822 | ||||||
chr4:168155822
|
G | GATATATC others(77): Show |
1 | a0002c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.196-6700_196-6699i others(86): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155822 | |||||
chr4:168155822
|
G | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(25): Show | 29 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-6706G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155822 | ||||||
chr4:168155822
|
GATATATG others(26): Show |
G | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6685_196-6653d others(35): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155822 | |||||
chr4:168155825
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196-6703A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155825 | ||||||
chr4:168155829
|
G | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6699G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155829 | ||||||
chr4:168155829
|
G | C | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-6699G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155829 | ||||||
chr4:168155829
|
G | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(146): Show | 152 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.196-6699G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155829 | ||||||
chr4:168155831
|
TATATCAT others(5): Show |
T | 8 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 9 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-6692_196-6681d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155831 | |||||
chr4:168155836
|
C | A | 30 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(27): Show | 31 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.196-6692C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155836 | ||||||
chr4:168155836
|
C | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-6692C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155836 | ||||||
chr4:168155836
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(115): Show | 120 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.196-6692C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155836 | ||||||
chr4:168155838
|
TATATA | T | 7 | a0001c0001t0001g0219a0001c0003t0001g0032a0001c0003t0001g0142others(4): Show | 7 | HG00639.hp2 HG01069.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.196-6679_196-6675d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155838 | |||||
chr4:168155842
|
T | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(25): Show | 29 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-6686T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155842 | ||||||
chr4:168155843
|
A | G | 2 | a0001c0003t0001g0014a0003c0004t0001g0223 | 2 | HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6685A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155843 | ||||||
chr4:168155843
|
A | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 39 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.196-6685A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155843 | ||||||
chr4:168155848
|
A | ATG | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.196-6680_196-6679i others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155848 | ||||||
chr4:168155848
|
A | G | 4 | a0001c0001t0001g0198a0001c0001t0001g0219a0001c0003t0001g0032others(1): Show | 4 | HG01069.hp1 HG01123.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6680A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155848 | ||||||
chr4:168155848
|
A | T | 1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-6680A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155848 | ||||||
chr4:168155848
|
AATATATC others(7): Show |
A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-6666_196-6653d others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155848 | |||||
chr4:168155848
|
AATATATC others(82): Show |
A | 96 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(93): Show | 98 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.196-6673_196-6585d others(91): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155848 | |||||
chr4:168155855
|
C | A | 3 | a0001c0001t0001g0278a0001c0003t0001g0014a0002c0002t0001g0108 | 3 | HG02886.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6673C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155855 | ||||||
chr4:168155855
|
C | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 9 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-6673C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155855 | ||||||
chr4:168155855
|
C | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-6673C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155855 | ||||||
chr4:168155862
|
G | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6666G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155862 | ||||||
chr4:168155862
|
G | C | 5 | a0001c0001t0001g0278a0003c0004t0001g0096a0003c0004t0001g0220others(2): Show | 5 | HG02717.hp2 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6666G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155862 | ||||||
chr4:168155862
|
G | GATATATC others(47): Show |
2 | a0002c0002t0001g0120a0002c0002t0001g0121 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.196-6607_196-6554d others(56): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155862 | |||||
chr4:168155862
|
G | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 11 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-6666G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155862 | ||||||
chr4:168155862
|
GATATATC others(47): Show |
G | 8 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(5): Show | 8 | HG02132.hp2 NA18944.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-6607_196-6554d others(56): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155862 | |||||
chr4:168155863
|
ATATATCA others(40): Show |
A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196-6659_196-6613d others(49): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155863 | |||||
chr4:168155864
|
T | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6664T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155864 | ||||||
chr4:168155864
|
TATATCAT others(52): Show |
T | 1 | a0003c0004t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.196-6659_196-6601d others(61): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155864 | |||||
chr4:168155869
|
C | A | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6659C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155869 | ||||||
chr4:168155869
|
C | G | 16 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 17 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-6659C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155869 | ||||||
chr4:168155869
|
C | T | 29 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0217others(26): Show | 29 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-6659C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155869 | ||||||
chr4:168155871
|
TATATTAT others(45): Show |
T | 4 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0224others(1): Show | 4 | HG02717.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.196-6652_196-6601d others(54): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155871 | |||||
chr4:168155874
|
ATTATATG others(2): Show |
A | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6653_196-6645d others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155874 | ||||||
chr4:168155876
|
T | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0003t0001g0014 | 3 | HG01891.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6652T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155876 | ||||||
chr4:168155878
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-6650T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155878 | ||||||
chr4:168155880
|
TGTTATAT others(4): Show |
T | 1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-6647_196-6637d others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155880 | ||||||
chr4:168155881
|
G | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 25 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.196-6647G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155881 | ||||||
chr4:168155882
|
TTA | T | 5 | a0001c0001t0001g0219a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01069.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6639_196-6638d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155882 | |||||
chr4:168155883
|
T | A | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6645T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155883 | ||||||
chr4:168155883
|
T | G | 11 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 12 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-6645T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155883 | ||||||
chr4:168155885
|
T | A | 5 | a0001c0001t0001g0219a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01069.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6643T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155885 | ||||||
chr4:168155885
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6643T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155885 | ||||||
chr4:168155885
|
TATATAAT others(52): Show |
T | 28 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(25): Show | 29 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-6637_196-6579d others(61): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155885 | |||||
chr4:168155890
|
A | T | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6638A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155890 | ||||||
chr4:168155891
|
A | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-6637A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155891 | ||||||
chr4:168155892
|
T | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-6636T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155892 | ||||||
chr4:168155895
|
ATGATATA others(35): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.196-6632_196-6591d others(44): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155895 | ||||||
chr4:168155896
|
T | A | 11 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 12 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-6632T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155896 | ||||||
chr4:168155897
|
G | A | 5 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0003t0001g0014others(2): Show | 5 | HG01069.hp1 HG01891.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-6631G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155897 | ||||||
chr4:168155897
|
G | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6631G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155897 | ||||||
chr4:168155897
|
G | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 12 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.196-6631G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155897 | ||||||
chr4:168155903
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6625T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155903 | ||||||
chr4:168155903
|
T | G | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6625T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155903 | ||||||
chr4:168155904
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-6624C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155904 | ||||||
chr4:168155904
|
C | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6624C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155904 | ||||||
chr4:168155904
|
C | T | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6624C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155904 | ||||||
chr4:168155905
|
ATATAT | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 17 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.196-6612_196-6608d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155905 | |||||
chr4:168155910
|
T | A | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6618T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155910 | ||||||
chr4:168155911
|
TATATTAT others(5): Show |
T | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.196-6612_196-6601d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155911 | |||||
chr4:168155915
|
TTATATAT others(23): Show |
T | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6607_196-6578d others(32): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155915 | |||||
chr4:168155916
|
T | C | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6612T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155916 | ||||||
chr4:168155916
|
T | G | 22 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 24 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.196-6612T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155916 | ||||||
chr4:168155923
|
C | G | 2 | a0001c0003t0001g0014a0002c0002t0001g0108 | 2 | HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6605C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155923 | ||||||
chr4:168155923
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 16 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.196-6605C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155923 | ||||||
chr4:168155930
|
T | C | 1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196-6598T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155930 | ||||||
chr4:168155935
|
G | A | 3 | a0001c0001t0001g0117a0001c0003t0001g0014a0002c0002t0001g0108 | 3 | HG02886.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196-6593G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155935 | ||||||
chr4:168155937
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6591T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155937 | ||||||
chr4:168155939
|
TATATA | T | 10 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0003t0001g0032others(7): Show | 10 | HG01069.hp1 HG01928.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.196-6583_196-6579d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155939 | |||||
chr4:168155940
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6588A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155940 | ||||||
chr4:168155942
|
A | G | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6586A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155942 | ||||||
chr4:168155944
|
A | T | 1 | a0001c0003t0001g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196-6584A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155944 | ||||||
chr4:168155945
|
A | ATATATGA others(17): Show |
1 | a0006c0007t0001g0015 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.196-6559_196-6536d others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155945 | |||||
chr4:168155945
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6583A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155945 | ||||||
chr4:168155952
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6576A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155952 | ||||||
chr4:168155957
|
T | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.196-6571T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155957 | ||||||
chr4:168155963
|
A | G | 4 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG01891.hp2 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6565A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155963 | ||||||
chr4:168155964
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6564T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155964 | ||||||
chr4:168155970
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.196-6558T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155970 | ||||||
chr4:168155975
|
G | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-6553G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155975 | ||||||
chr4:168155983
|
ATATAT | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0177 | 3 | NA18951.hp2 NA18968.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.196-6540_196-6536d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168155983 | |||||
chr4:168155993
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.196-6535C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155993 | ||||||
chr4:168155994
|
A | T | 1 | a0002c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.196-6534A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168155994 | ||||||
chr4:168156007
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.196-6521T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156007 | ||||||
chr4:168156010
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6518G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156010 | ||||||
chr4:168156010
|
G | GTTATATA others(100): Show |
1 | a0002c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.196-6510_196-6509i others(109): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156010 | |||||
chr4:168156019
|
A | C | 2 | a0001c0001t0001g0117a0002c0002t0001g0178 | 2 | HG01928.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196-6509A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156019 | ||||||
chr4:168156034
|
G | GTATTATA others(38): Show |
14 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(11): Show | 14 | HG01496.hp2 HG01943.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.196-6490_196-6446d others(47): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156034 | |||||
chr4:168156034
|
G | T | 2 | a0001c0001t0001g0117a0002c0002t0001g0178 | 2 | HG01928.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196-6494G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156034 | ||||||
chr4:168156037
|
T | TTATATTA others(21): Show |
1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196-6478_196-6451d others(30): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156037 | |||||
chr4:168156037
|
T | TTATATTA others(49): Show |
4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-6451_196-6450i others(58): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156037 | |||||
chr4:168156037
|
TTATATTA | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6471_196-6465d others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156037 | |||||
chr4:168156042
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6486T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156042 | ||||||
chr4:168156046
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6482A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156046 | ||||||
chr4:168156047
|
T | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6481T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156047 | ||||||
chr4:168156050
|
T | A | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG02451.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-6478T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156050 | ||||||
chr4:168156055
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196-6473A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156055 | ||||||
chr4:168156063
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6465T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156063 | ||||||
chr4:168156064
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.196-6464C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156064 | ||||||
chr4:168156064
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6464C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156064 | ||||||
chr4:168156067
|
A | ATATTATA others(63): Show |
1 | a0001c0001t0001g0231 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196-6450_196-6449i others(72): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156067 | |||||
chr4:168156067
|
A | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6461A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156067 | ||||||
chr4:168156101
|
A | ATAT | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6425_196-6424i others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156101 | |||||
chr4:168156103
|
A | AT | 13 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-6425_196-6424i others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156103 | ||||||
chr4:168156103
|
A | ATTATATA others(1): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0217others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6425_196-6424i others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156103 | ||||||
chr4:168156104
|
A | T | 17 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 18 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.196-6424A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156104 | ||||||
chr4:168156108
|
T | TATAATAT others(39): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6420_196-6419i others(48): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156108 | ||||||
chr4:168156108
|
T | TATAATAT others(39): Show |
6 | a0001c0001t0001g0215a0001c0001t0001g0221a0001c0001t0001g0222others(3): Show | 6 | HG02055.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-6420_196-6419i others(48): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156108 | ||||||
chr4:168156108
|
T | TTTATTAT others(7): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0217others(1): Show | 4 | HG01891.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6419_196-6418i others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156108 | |||||
chr4:168156109
|
T | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6419T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156109 | ||||||
chr4:168156118
|
T | TATA | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6410_196-6409i others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156118 | ||||||
chr4:168156124
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6404T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156124 | ||||||
chr4:168156124
|
T | TA | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6404_196-6403i others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156124 | ||||||
chr4:168156127
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6401T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156127 | ||||||
chr4:168156130
|
A | AATATT | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6398_196-6397i others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156130 | ||||||
chr4:168156133
|
T | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.196-6395T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156133 | ||||||
chr4:168156137
|
A | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02486.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.196-6391A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156137 | ||||||
chr4:168156141
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6387A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156141 | ||||||
chr4:168156143
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6385A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156143 | ||||||
chr4:168156144
|
A | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6384A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156144 | ||||||
chr4:168156145
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6383A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156145 | ||||||
chr4:168156147
|
A | ATTT | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6381_196-6380i others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156147 | ||||||
chr4:168156147
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6381A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156147 | ||||||
chr4:168156150
|
A | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6378A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156150 | ||||||
chr4:168156151
|
T | C | 1 | a0007c0010t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.196-6377T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156151 | ||||||
chr4:168156155
|
T | TTTA | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6372_196-6371i others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156155 | |||||
chr4:168156162
|
T | TAA | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(152): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.196-6366_196-6365i others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156162 | ||||||
chr4:168156165
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6363T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156165 | ||||||
chr4:168156167
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6361T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156167 | ||||||
chr4:168156169
|
T | TA | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6358dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156169 | |||||
chr4:168156171
|
T | A | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6357T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156171 | ||||||
chr4:168156171
|
T | TTATATTA | 11 | a0002c0002t0001g0115a0002c0002t0001g0130a0002c0002t0001g0139others(8): Show | 11 | HG00140.hp2 HG00639.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-6337_196-6331d others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156171 | |||||
chr4:168156171
|
T | TTATATTA others(7): Show |
86 | a0002c0002t0001g0003a0002c0002t0001g0006a0002c0002t0001g0007others(83): Show | 88 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.196-6344_196-6331d others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156171 | |||||
chr4:168156171
|
T | TTATATTA others(14): Show |
3 | a0002c0002t0001g0040a0002c0002t0001g0161a0002c0002t0001g0232 | 3 | HG02723.hp2 HG03139.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.196-6351_196-6331d others(23): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156171 | |||||
chr4:168156172
|
T | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6356T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156172 | ||||||
chr4:168156176
|
T | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6352T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156176 | ||||||
chr4:168156177
|
T | A | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6351T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156177 | ||||||
chr4:168156178
|
A | T | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196-6350A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156178 | ||||||
chr4:168156183
|
T | TTATA | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.196-6341_196-6338d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(94): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0229 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.196-6338_196-6337i others(103): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(2): Show |
88 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.196-6338_196-6330d others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(4): Show |
1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196-6336_196-6335i others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(4): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(10): Show | 14 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.196-6340_196-6330d others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(34): Show |
29 | a0001c0001t0001g0039a0001c0001t0001g0198a0001c0001t0001g0199others(26): Show | 29 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-6330_196-6329i others(43): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156183
|
T | TTATATAT others(9): Show |
3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6331_196-6330i others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156183 | |||||
chr4:168156190
|
T | TTA | 4 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 5 | HG00735.hp2 HG01081.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-6331_196-6330d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156190 | |||||
chr4:168156191
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0229 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.196-6337T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156191 | ||||||
chr4:168156191
|
T | TATATATA others(34): Show |
2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.196-6330_196-6329i others(43): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156191 | |||||
chr4:168156193
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196-6335T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156193 | ||||||
chr4:168156198
|
A | ATATTATA others(4): Show |
15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(12): Show | 15 | HG00099.hp2 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-6330_196-6329i others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156198 | ||||||
chr4:168156198
|
A | T | 18 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(15): Show | 18 | HG01496.hp2 HG01884.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.196-6330A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156198 | ||||||
chr4:168156199
|
A | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 6 | HG00735.hp2 HG01081.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-6329A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156199 | ||||||
chr4:168156203
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.196-6325A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156203 | ||||||
chr4:168156204
|
T | TTATATAT others(87): Show |
1 | a0002c0002t0001g0188 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.196-6324_196-6323i others(96): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156204 | ||||||
chr4:168156206
|
T | TTATA | 4 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 5 | HG00735.hp2 HG01081.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.196-6320_196-6317d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156206 | |||||
chr4:168156206
|
T | TTATATTA others(95): Show |
11 | a0002c0002t0001g0081a0002c0002t0001g0146a0002c0002t0001g0153others(8): Show | 11 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.196-6312_196-6311i others(104): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156206 | |||||
chr4:168156206
|
T | TTATATTA others(67): Show |
3 | a0002c0002t0001g0143a0002c0002t0001g0155a0002c0002t0001g0181 | 3 | HG02155.hp1 NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.196-6312_196-6311i others(76): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156206 | |||||
chr4:168156220
|
A | ATAT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.196-6307_196-6305d others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156220 | |||||
chr4:168156227
|
T | TTATATTA others(29): Show |
1 | a0001c0003t0001g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.196-6286_196-6285i others(38): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156227 | |||||
chr4:168156230
|
T | TATTATAT others(41): Show |
1 | a0001c0003t0001g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.196-6270_196-6269i others(50): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156230 | |||||
chr4:168156264
|
A | ATATATTA others(22): Show |
1 | a0002c0002t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.196-6239_196-6211d others(31): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156264 | |||||
chr4:168156281
|
G | T | 1 | a0001c0003t0001g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.196-6247G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156281 | ||||||
chr4:168156283
|
A | ATATATTA others(3): Show |
1 | a0002c0002t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.196-6234_196-6225d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156283 | |||||
chr4:168156283
|
ATATAT | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(105): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.196-6229_196-6225d others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156283 | |||||
chr4:168156288
|
T | TTATATAT others(25): Show |
28 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 29 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.196-6235_196-6234i others(34): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156288 | |||||
chr4:168156288
|
T | TTATATAT others(25): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 7 | HG01123.hp2 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.196-6235_196-6234i others(34): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156288 | |||||
chr4:168156291
|
T | G | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6237T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156291 | ||||||
chr4:168156302
|
A | AT | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6225dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156302 | |||||
chr4:168156306
|
A | AT | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6222_196-6221i others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156306 | ||||||
chr4:168156319
|
A | C | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-6209A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156319 | ||||||
chr4:168156329
|
T | G | 1 | a0002c0002t0001g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.196-6199T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156329 | ||||||
chr4:168156338
|
GTA | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-6184_196-6183d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156338 | |||||
chr4:168156350
|
T | G | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-6178T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156350 | ||||||
chr4:168156353
|
A | AATATATT others(37): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-6154_196-6111d others(46): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 168156353 | |||||
chr4:168156391
|
T | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.196-6137T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156391 | ||||||
chr4:168156403
|
T | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 138 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.196-6125T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156403 | ||||||
chr4:168156420
|
T | C | 24 | a0001c0003t0001g0013a0001c0003t0001g0016a0001c0003t0001g0020others(21): Show | 24 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.196-6108T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156420 | ||||||
chr4:168156456
|
A | G | 19 | a0002c0002t0001g0081a0002c0002t0001g0108a0002c0002t0001g0115others(16): Show | 19 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-6072A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156456 | ||||||
chr4:168156535
|
A | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-5993A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156535 | ||||||
chr4:168156616
|
G | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-5912G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156616 | ||||||
chr4:168156652
|
C | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.196-5876C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156652 | ||||||
chr4:168156755
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.196-5773G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156755 | ||||||
chr4:168156774
|
G | A | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-5754G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156774 | ||||||
chr4:168156793
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.196-5735A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156793 | ||||||
chr4:168156798
|
C | T | 3 | a0002c0002t0001g0270a0006c0007t0001g0015a0006c0007t0001g0268 | 3 | HG00639.hp2 HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.196-5730C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156798 | ||||||
chr4:168156799
|
G | A | 8 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(5): Show | 8 | HG01346.hp1 HG01993.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5729G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156799 | ||||||
chr4:168156799
|
G | T | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196-5729G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156799 | ||||||
chr4:168156862
|
T | C | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196-5666T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156862 | ||||||
chr4:168156863
|
G | T | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196-5665G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156863 | ||||||
chr4:168156875
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196-5653G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156875 | ||||||
chr4:168156878
|
G | C | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-5650G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156878 | ||||||
chr4:168156919
|
A | G | 2 | a0002c0002t0001g0274a0002c0002t0001g0275 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.196-5609A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156919 | ||||||
chr4:168156921
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.196-5607C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168156921 | ||||||
chr4:168157025
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-5503G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157025 | ||||||
chr4:168157089
|
A | C | 1 | a0001c0003t0001g0013 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.196-5439A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157089 | ||||||
chr4:168157103
|
TG | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.196-5424delG | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157103 | ||||||
chr4:168157105
|
A | G | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-5423A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157105 | ||||||
chr4:168157268
|
TA | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0055others(2): Show | 6 | HG00738.hp1 HG01106.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-5259delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157268 | ||||||
chr4:168157271
|
T | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-5257T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157271 | ||||||
chr4:168157293
|
A | G | 33 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(30): Show | 34 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.196-5235A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157293 | ||||||
chr4:168157334
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.196-5194C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157334 | ||||||
chr4:168157404
|
A | G | 1 | a0001c0003t0001g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.196-5124A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157404 | ||||||
chr4:168157412
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.196-5116C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157412 | ||||||
chr4:168157458
|
G | A | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG00140.hp1 HG00639.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.196-5070G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157458 | ||||||
chr4:168157461
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196-5067T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157461 | ||||||
chr4:168157629
|
C | T | 5 | a0002c0002t0001g0006a0002c0002t0001g0226a0002c0002t0001g0232others(2): Show | 6 | HG02280.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-4899C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157629 | ||||||
chr4:168157656
|
G | T | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-4872G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157656 | ||||||
chr4:168157721
|
T | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-4807T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157721 | ||||||
chr4:168157798
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196-4730T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157798 | ||||||
chr4:168157804
|
A | G | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.196-4724A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157804 | ||||||
chr4:168157866
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.196-4662C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168157866 | ||||||
chr4:168158184
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.196-4344C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168158184 | ||||||
chr4:168158418
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196-4110T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168158418 | ||||||
chr4:168158499
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.196-4029C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168158499 | ||||||
chr4:168158644
|
A | T | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-3884A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168158644 | ||||||
chr4:168158880
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.196-3648G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168158880 | ||||||
chr4:168159223
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.196-3305C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159223 | ||||||
chr4:168159332
|
A | G | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.196-3196A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159332 | ||||||
chr4:168159751
|
T | G | 1 | a0002c0002t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.196-2777T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159751 | ||||||
chr4:168159882
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.196-2646G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159882 | ||||||
chr4:168159887
|
A | C | 29 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0045others(26): Show | 30 | HG00738.hp1 HG01081.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.196-2641A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159887 | ||||||
chr4:168159938
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196-2590T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168159938 | ||||||
chr4:168160037
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(171): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.196-2491T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160037 | ||||||
chr4:168160038
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.196-2490A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160038 | ||||||
chr4:168160171
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.196-2357C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160171 | ||||||
chr4:168160308
|
C | T | 1 | a0001c0003t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196-2220C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160308 | ||||||
chr4:168160779
|
T | C | 1 | a0002c0002t0001g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.196-1749T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160779 | ||||||
chr4:168160849
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.196-1679C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160849 | ||||||
chr4:168160886
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.196-1642T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168160886 | ||||||
chr4:168161372
|
C | T | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196-1156C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168161372 | ||||||
chr4:168161400
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.196-1128T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168161400 | ||||||
chr4:168161464
|
C | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.196-1064C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168161464 | ||||||
chr4:168161475
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.196-1053G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168161475 | ||||||
chr4:168161738
|
T | C | 19 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0239others(16): Show | 19 | HG00438.hp2 HG01884.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.196-790T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168161738 | ||||||
chr4:168162055
|
C | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0036 | 3 | HG01081.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196-473C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168162055 | ||||||
chr4:168162147
|
T | C | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196-381T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | 168162147 | ||||||
chr4:168162826
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.309+185C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168162826 | ||||||
chr4:168162839
|
T | C | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+198T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168162839 | ||||||
chr4:168162963
|
T | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(35): Show | 39 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.309+322T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168162963 | ||||||
chr4:168163104
|
G | A | 1 | a0002c0002t0001g0144 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.309+463G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163104 | ||||||
chr4:168163126
|
AT | A | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG00140.hp1 HG00738.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+496delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 168163126 | |||||
chr4:168163217
|
T | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.309+576T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163217 | ||||||
chr4:168163490
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | NA18970.hp1 NA19003.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-708G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163490 | ||||||
chr4:168163500
|
CAT | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.310-697_310-696del others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163500 | ||||||
chr4:168163552
|
A | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(3): Show | 7 | HG01123.hp2 HG02258.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-646A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163552 | ||||||
chr4:168163602
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(274): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.310-596G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163602 | ||||||
chr4:168163648
|
T | TA | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.310-544dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr4 | 168163648 | |||||
chr4:168163722
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.310-476G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163722 | ||||||
chr4:168163909
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.310-289C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 4/11 | chr4 | 168163909 | ||||||
chr4:168164442
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.400+154C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168164442 | ||||||
chr4:168164670
|
G | A | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+382G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168164670 | ||||||
chr4:168164693
|
C | T | 1 | a0002c0002t0001g0154 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.400+405C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168164693 | ||||||
chr4:168164704
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.400+416A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168164704 | ||||||
chr4:168165009
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.401-238A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168165009 | ||||||
chr4:168165165
|
G | T | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401-82G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 5/11 | chr4 | 168165165 | ||||||
chr4:168165389
|
C | CAAAA | 14 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(11): Show | 14 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.480+77_480+80dupAA others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168165389 | |||||
chr4:168165389
|
CA | C | 8 | a0001c0001t0001g0217a0001c0001t0001g0261a0001c0001t0001g0264others(5): Show | 8 | HG00140.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+80delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168165389 | |||||
chr4:168165389
|
CAA | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.480+79_480+80delAA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168165389 | |||||
chr4:168165389
|
CAAA | C | 23 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0071others(20): Show | 23 | HG00735.hp1 HG01346.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.480+78_480+80delAA others(1): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168165389 | |||||
chr4:168165559
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.480+233C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165559 | ||||||
chr4:168165670
|
ATTTCTTT others(1): Show |
A | 5 | a0002c0002t0001g0006a0002c0002t0001g0226a0002c0002t0001g0232others(2): Show | 6 | HG02280.hp1 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+360_480+367del others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168165670 | |||||
chr4:168165708
|
G | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.480+382G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165708 | ||||||
chr4:168165733
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480+407G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165733 | ||||||
chr4:168165824
|
G | A | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.480+498G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165824 | ||||||
chr4:168165874
|
A | G | 1 | a0002c0002t0001g0157 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.480+548A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165874 | ||||||
chr4:168165920
|
G | A | 2 | a0002c0002t0001g0104a0002c0002t0001g0105 | 2 | NA18960.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.480+594G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168165920 | ||||||
chr4:168166164
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.480+838G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166164 | ||||||
chr4:168166180
|
T | C | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+854T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166180 | ||||||
chr4:168166334
|
AT | A | 4 | a0002c0002t0001g0108a0002c0002t0001g0115a0002c0002t0001g0200others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+1011delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166334 | |||||
chr4:168166424
|
C | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+1098C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166424 | ||||||
chr4:168166452
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.480+1126C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166452 | ||||||
chr4:168166488
|
T | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+1162T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166488 | ||||||
chr4:168166490
|
C | T | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+1164C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166490 | ||||||
chr4:168166497
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.480+1171A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166497 | ||||||
chr4:168166505
|
A | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480+1179A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166505 | ||||||
chr4:168166532
|
C | T | 4 | a0004c0005t0001g0043a0004c0005t0001g0048a0004c0005t0001g0049others(1): Show | 4 | NA18951.hp1 NA18974.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1206C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166532 | ||||||
chr4:168166631
|
C | CGT | 18 | a0002c0002t0001g0006a0002c0002t0001g0070a0002c0002t0001g0104others(15): Show | 19 | HG00621.hp1 HG01099.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.480+1354_480+1355d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
C | CGTGT | 4 | a0002c0002t0001g0133a0002c0002t0001g0139a0002c0002t0001g0163others(1): Show | 4 | HG01169.hp1 HG01261.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+1352_480+1355d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGT | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0057others(37): Show | 41 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.480+1354_480+1355d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGT | C | 52 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(49): Show | 53 | HG01069.hp2 HG01243.hp1 HG01258.hp1 others(50): Show |
intron_variant | MODIFIER | c.480+1352_480+1355d others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGT | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0058others(43): Show | 47 | HG00323.hp1 HG00741.hp2 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.480+1350_480+1355d others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(1): Show |
C | 35 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(32): Show | 36 | HG00438.hp2 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.480+1348_480+1355d others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.480+1346_480+1355d others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0111 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.480+1344_480+1355d others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(7): Show |
C | 13 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(10): Show | 14 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.480+1342_480+1355d others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480+1340_480+1355d others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(11): Show |
C | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+1338_480+1355d others(20): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166631
|
CGTGTGTG others(17): Show |
C | 6 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(3): Show | 6 | HG01884.hp1 HG01993.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+1332_480+1355d others(26): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168166631 | |||||
chr4:168166797
|
T | C | 1 | a0002c0002t0001g0044 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.480+1471T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168166797 | ||||||
chr4:168167347
|
A | T | 1 | a0002c0002t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.480+2021A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167347 | ||||||
chr4:168167471
|
G | T | 4 | a0002c0002t0001g0125a0002c0002t0001g0126a0002c0002t0001g0165others(1): Show | 4 | HG00438.hp1 HG00621.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+2145G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167471 | ||||||
chr4:168167486
|
CA | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0251others(3): Show | 6 | HG00438.hp2 HG02132.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+2162delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168167486 | |||||
chr4:168167535
|
A | G | 1 | a0001c0003t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+2209A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167535 | ||||||
chr4:168167608
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480+2282G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167608 | ||||||
chr4:168167754
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 139 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.480+2428C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167754 | ||||||
chr4:168167858
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480+2532G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167858 | ||||||
chr4:168167870
|
G | C | 1 | a0002c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+2544G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167870 | ||||||
chr4:168167940
|
T | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0201 | 2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.480+2614T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168167940 | ||||||
chr4:168168111
|
T | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.480+2785T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168111 | ||||||
chr4:168168140
|
T | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0080 | 2 | HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.480+2814T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168140 | ||||||
chr4:168168167
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.480+2841T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168167 | ||||||
chr4:168168429
|
T | C | 2 | a0002c0002t0001g0274a0002c0002t0001g0275 | 2 | HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.480+3103T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168429 | ||||||
chr4:168168442
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3116G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168442 | ||||||
chr4:168168514
|
G | T | 1 | a0001c0001t0001g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.480+3188G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168514 | ||||||
chr4:168168541
|
T | C | 2 | a0001c0009t0001g0207a0001c0009t0001g0208 | 2 | HG00099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.480+3215T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168541 | ||||||
chr4:168168566
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0228 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.480+3240C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168566 | ||||||
chr4:168168610
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(2): Show | 5 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3284G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168610 | ||||||
chr4:168168665
|
C | T | 3 | a0001c0001t0001g0117a0002c0002t0001g0176a0002c0002t0001g0187 | 3 | NA18522.hp1 NA19063.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.480+3339C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168665 | ||||||
chr4:168168756
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.480+3430A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168756 | ||||||
chr4:168168823
|
C | G | 3 | a0002c0002t0001g0108a0002c0002t0001g0200a0002c0002t0001g0201 | 3 | HG02647.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.480+3497C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168823 | ||||||
chr4:168168877
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+3551A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168877 | ||||||
chr4:168168892
|
G | C | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480+3566G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168892 | ||||||
chr4:168168930
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.480+3604T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168930 | ||||||
chr4:168168946
|
T | G | 1 | a0002c0002t0001g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.480+3620T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168946 | ||||||
chr4:168168949
|
C | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+3623C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168168949 | ||||||
chr4:168169128
|
G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.480+3802G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169128 | ||||||
chr4:168169215
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+3889T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169215 | ||||||
chr4:168169393
|
C | A | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.480+4067C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169393 | ||||||
chr4:168169512
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.480+4186T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169512 | ||||||
chr4:168169515
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+4189G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169515 | ||||||
chr4:168169656
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.480+4330A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169656 | ||||||
chr4:168169740
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.480+4414G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169740 | ||||||
chr4:168169777
|
C | G | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+4451C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169777 | ||||||
chr4:168169818
|
C | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+4492C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169818 | ||||||
chr4:168169951
|
G | A | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+4625G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168169951 | ||||||
chr4:168170114
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.480+4788G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170114 | ||||||
chr4:168170126
|
A | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+4800A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170126 | ||||||
chr4:168170174
|
A | G | 1 | a0002c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+4848A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170174 | ||||||
chr4:168170639
|
G | A | 2 | a0001c0003t0001g0014a0001c0003t0001g0038 | 2 | HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.480+5313G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170639 | ||||||
chr4:168170672
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+5346T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170672 | ||||||
chr4:168170798
|
A | G | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.480+5472A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170798 | ||||||
chr4:168170831
|
AG | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+5506delG | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170831 | ||||||
chr4:168170835
|
T | A | 23 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 24 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.480+5509T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170835 | ||||||
chr4:168170861
|
G | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.480+5535G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170861 | ||||||
chr4:168170900
|
A | G | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.480+5574A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170900 | ||||||
chr4:168170912
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.480+5586G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168170912 | ||||||
chr4:168171150
|
A | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.480+5824A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168171150 | ||||||
chr4:168171191
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+5865T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168171191 | ||||||
chr4:168171325
|
T | G | 1 | a0002c0002t0001g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.480+5999T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168171325 | ||||||
chr4:168171529
|
G | T | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+6203G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168171529 | ||||||
chr4:168171763
|
C | T | 1 | a0002c0002t0001g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.481-5977C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168171763 | ||||||
chr4:168172067
|
C | T | 1 | a0002c0002t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.481-5673C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172067 | ||||||
chr4:168172176
|
G | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-5564G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172176 | ||||||
chr4:168172300
|
T | G | 1 | a0001c0001t0001g0101 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.481-5440T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172300 | ||||||
chr4:168172335
|
A | T | 1 | a0002c0002t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.481-5405A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172335 | ||||||
chr4:168172424
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.481-5316C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172424 | ||||||
chr4:168172598
|
G | A | 12 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.481-5142G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172598 | ||||||
chr4:168172610
|
T | C | 1 | a0001c0011t0001g0216 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.481-5130T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172610 | ||||||
chr4:168172637
|
C | T | 15 | a0002c0002t0001g0081a0002c0002t0001g0143a0002c0002t0001g0146others(12): Show | 15 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-5103C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172637 | ||||||
chr4:168172677
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.481-5063T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172677 | ||||||
chr4:168172786
|
AT | A | 25 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(22): Show | 25 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.481-4934delT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168172786 | |||||
chr4:168172786
|
ATT | A | 13 | a0001c0001t0001g0058a0001c0001t0001g0073a0001c0001t0001g0192others(10): Show | 13 | HG01109.hp2 HG02109.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-4935_481-4934d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168172786 | |||||
chr4:168172786
|
ATTT | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.481-4936_481-4934d others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168172786 | |||||
chr4:168172838
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-4902G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168172838 | ||||||
chr4:168173007
|
C | T | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-4733C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173007 | ||||||
chr4:168173024
|
A | G | 1 | a0002c0002t0001g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.481-4716A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173024 | ||||||
chr4:168173156
|
A | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-4584A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173156 | ||||||
chr4:168173157
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.481-4583T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173157 | ||||||
chr4:168173166
|
G | T | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-4574G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173166 | ||||||
chr4:168173233
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.481-4507G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173233 | ||||||
chr4:168173277
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.481-4463G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173277 | ||||||
chr4:168173362
|
T | G | 2 | a0002c0002t0001g0120a0002c0002t0001g0121 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.481-4378T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173362 | ||||||
chr4:168173602
|
T | C | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-4138T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173602 | ||||||
chr4:168173721
|
C | G | 1 | a0002c0002t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.481-4019C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173721 | ||||||
chr4:168173858
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.481-3882G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173858 | ||||||
chr4:168173923
|
C | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(52): Show | 57 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.481-3817C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168173923 | ||||||
chr4:168174072
|
C | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(50): Show | 55 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.481-3668C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174072 | ||||||
chr4:168174084
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(31): Show | 36 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.481-3656A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174084 | ||||||
chr4:168174448
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.481-3292C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174448 | ||||||
chr4:168174455
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.481-3285G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174455 | ||||||
chr4:168174604
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.481-3136G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174604 | ||||||
chr4:168174810
|
GAA | G | 7 | a0001c0001t0001g0117a0001c0001t0001g0217a0001c0001t0001g0218others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2928_481-2927d others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168174810 | |||||
chr4:168174935
|
T | A | 1 | a0001c0003t0001g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.481-2805T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168174935 | ||||||
chr4:168175019
|
A | C | 1 | a0002c0002t0001g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.481-2721A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175019 | ||||||
chr4:168175055
|
T | C | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2685T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175055 | ||||||
chr4:168175194
|
G | A | 8 | a0002c0002t0001g0081a0002c0002t0001g0125a0002c0002t0001g0126others(5): Show | 8 | HG00438.hp1 HG00621.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2546G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175194 | ||||||
chr4:168175244
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481-2496C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175244 | ||||||
chr4:168175357
|
A | G | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2383A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175357 | ||||||
chr4:168175580
|
C | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-2160C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175580 | ||||||
chr4:168175803
|
G | A | 24 | a0001c0003t0001g0013a0001c0003t0001g0016a0001c0003t0001g0020others(21): Show | 24 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.481-1937G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175803 | ||||||
chr4:168175845
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.481-1895T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168175845 | ||||||
chr4:168176008
|
A | AT | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.481-1731dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 168176008 | |||||
chr4:168176277
|
C | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(16): Show | 20 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.481-1463C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176277 | ||||||
chr4:168176342
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.481-1398A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176342 | ||||||
chr4:168176527
|
C | T | 5 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG01884.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-1213C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176527 | ||||||
chr4:168176743
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-997G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176743 | ||||||
chr4:168176785
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(28): Show | 33 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.481-955G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176785 | ||||||
chr4:168176928
|
A | G | 1 | a0002c0002t0001g0105 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481-812A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176928 | ||||||
chr4:168176935
|
G | A | 1 | a0001c0003t0001g0037 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.481-805G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176935 | ||||||
chr4:168176993
|
C | T | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.481-747C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168176993 | ||||||
chr4:168177091
|
T | C | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01109.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.481-649T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168177091 | ||||||
chr4:168177181
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(24): Show | 29 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.481-559A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168177181 | ||||||
chr4:168177197
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-543C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168177197 | ||||||
chr4:168177295
|
G | C | 34 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(31): Show | 35 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.481-445G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168177295 | ||||||
chr4:168177565
|
C | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.481-175C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 6/11 | chr4 | 168177565 | ||||||
chr4:168177796
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03098.hp1 | splice_region_variant&intron_variant | LOW | c.534+3A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 7/11 | chr4 | 168177796 | ||||||
chr4:168177821
|
T | G | 1 | a0001c0001t0001g0273 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.534+28T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 7/11 | chr4 | 168177821 | ||||||
chr4:168177833
|
G | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(49): Show | 54 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.534+40G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 7/11 | chr4 | 168177833 | ||||||
chr4:168178004
|
G | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.628+21G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178004 | ||||||
chr4:168178028
|
T | C | 1 | a0002c0002t0001g0139 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.628+45T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178028 | ||||||
chr4:168178377
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.628+394C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178377 | ||||||
chr4:168178431
|
C | G | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.628+448C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178431 | ||||||
chr4:168178532
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.628+549C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178532 | ||||||
chr4:168178597
|
C | CATA | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0215others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-608_629-606dup others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr4 | 168178597 | |||||
chr4:168178748
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.629-469C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178748 | ||||||
chr4:168178770
|
T | A | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.629-447T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178770 | ||||||
chr4:168178935
|
T | C | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-282T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168178935 | ||||||
chr4:168179113
|
T | C | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-104T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 8/11 | chr4 | 168179113 | ||||||
chr4:168179326
|
T | C | 1 | a0001c0003t0001g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.724+14T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179326 | ||||||
chr4:168179339
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.724+27A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179339 | ||||||
chr4:168179417
|
A | G | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+105A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179417 | ||||||
chr4:168179462
|
G | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.724+150G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179462 | ||||||
chr4:168179610
|
C | T | 7 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.724+298C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179610 | ||||||
chr4:168179649
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | NA18952.hp1 NA18991.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+337C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179649 | ||||||
chr4:168179779
|
TA | T | 4 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+468delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179779 | ||||||
chr4:168179894
|
T | C | 1 | a0002c0002t0001g0154 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.724+582T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168179894 | ||||||
chr4:168180007
|
G | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(76): Show | 82 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.724+695G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180007 | ||||||
chr4:168180061
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.724+749A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180061 | ||||||
chr4:168180090
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.724+778G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180090 | ||||||
chr4:168180147
|
T | C | 7 | a0001c0001t0001g0117a0001c0001t0001g0218a0001c0001t0001g0228others(4): Show | 7 | HG01884.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.724+835T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180147 | ||||||
chr4:168180153
|
T | C | 1 | a0002c0002t0001g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.724+841T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180153 | ||||||
chr4:168180315
|
A | G | 1 | a0002c0002t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.724+1003A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180315 | ||||||
chr4:168180709
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.725-974A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168180709 | ||||||
chr4:168181079
|
GTTAATAA others(36): Show |
G | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.725-603_725-561del others(43): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181079 | ||||||
chr4:168181162
|
C | T | 4 | a0004c0005t0001g0043a0004c0005t0001g0048a0004c0005t0001g0049others(1): Show | 4 | NA18951.hp1 NA18974.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.725-521C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181162 | ||||||
chr4:168181210
|
T | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-473T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181210 | ||||||
chr4:168181211
|
GAAACCCC others(29): Show |
G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-471_725-436del others(36): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181211 | ||||||
chr4:168181228
|
A | G | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-455A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181228 | ||||||
chr4:168181241
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.725-442G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181241 | ||||||
chr4:168181251
|
C | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-432C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181251 | ||||||
chr4:168181253
|
T | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-430T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181253 | ||||||
chr4:168181255
|
G | T | 4 | a0002c0002t0001g0270a0002c0012t0001g0113a0006c0007t0001g0015others(1): Show | 4 | HG00639.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-428G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181255 | ||||||
chr4:168181256
|
T | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-427T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181256 | ||||||
chr4:168181259
|
C | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-424C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181259 | ||||||
chr4:168181260
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.725-423G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181260 | ||||||
chr4:168181263
|
C | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-420C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181263 | ||||||
chr4:168181264
|
G | GGGGGGGG others(34): Show |
1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-419_725-418ins others(41): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181264 | ||||||
chr4:168181265
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-418C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181265 | ||||||
chr4:168181268
|
G | A | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-415G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181268 | ||||||
chr4:168181271
|
G | C | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-412G>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181271 | ||||||
chr4:168181272
|
T | G | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-411T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181272 | ||||||
chr4:168181273
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-410C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181273 | ||||||
chr4:168181274
|
C | A | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-409C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181274 | ||||||
chr4:168181275
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-408C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181275 | ||||||
chr4:168181277
|
G | T | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-406G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181277 | ||||||
chr4:168181281
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.725-402C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181281 | ||||||
chr4:168181309
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.725-374T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181309 | ||||||
chr4:168181330
|
G | T | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-353G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181330 | ||||||
chr4:168181334
|
T | C | 1 | a0002c0002t0001g0178 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.725-349T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181334 | ||||||
chr4:168181390
|
C | CAA | 44 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(41): Show | 45 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.725-277_725-276dup others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 168181390 | |||||
chr4:168181390
|
C | CAAA | 44 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(41): Show | 46 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.725-278_725-276dup others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 168181390 | |||||
chr4:168181398
|
A | T | 4 | a0002c0002t0001g0122a0002c0002t0001g0123a0002c0002t0001g0124others(1): Show | 4 | HG01891.hp2 HG02647.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-285A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181398 | ||||||
chr4:168181421
|
T | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0251others(4): Show | 7 | HG00438.hp2 HG02132.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.725-262T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181421 | ||||||
chr4:168181433
|
G | A | 5 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(2): Show | 5 | HG02717.hp2 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-250G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181433 | ||||||
chr4:168181541
|
T | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0019others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.725-142T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181541 | ||||||
chr4:168181640
|
T | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0209others(5): Show | 9 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.725-43T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 9/11 | chr4 | 168181640 | ||||||
chr4:168181810
|
C | T | 1 | a0002c0002t0001g0184 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.783+69C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168181810 | ||||||
chr4:168182031
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.783+290T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182031 | ||||||
chr4:168182318
|
A | AT | 51 | a0002c0002t0001g0007a0002c0002t0001g0060a0002c0002t0001g0063others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.783+607dupT | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATT | 34 | a0001c0001t0001g0117a0001c0001t0001g0278a0002c0002t0001g0003others(31): Show | 35 | HG00438.hp1 HG00741.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.783+606_783+607dup others(2): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTT | 12 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0276others(9): Show | 12 | HG00099.hp1 HG01109.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.783+605_783+607dup others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTT | 17 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0078others(14): Show | 17 | HG00140.hp1 HG00639.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.783+604_783+607dup others(4): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTT | 27 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0051others(24): Show | 27 | HG00738.hp1 HG01081.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.783+603_783+607dup others(5): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTT | 24 | a0001c0001t0001g0019a0001c0001t0001g0046a0001c0001t0001g0067others(21): Show | 24 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.783+602_783+607dup others(6): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT | 21 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0055others(18): Show | 22 | HG00735.hp1 HG01106.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.783+601_783+607dup others(7): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(1): Show |
34 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0039others(31): Show | 35 | HG00438.hp2 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.783+600_783+607dup others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0213others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+599_783+607dup others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.783+598_783+607dup others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0198a0006c0007t0001g0015a0006c0007t0001g0268 | 3 | HG00639.hp2 HG01123.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.783+596_783+607dup others(12): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0005a0002c0002t0001g0200 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.783+595_783+607dup others(13): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0199a0002c0002t0001g0201 | 2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.783+594_783+607dup others(14): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0215a0001c0001t0001g0221a0001c0001t0001g0225others(1): Show | 4 | HG02145.hp2 HG02717.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+593_783+607dup others(15): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0001g0222a0001c0001t0001g0227a0001c0001t0001g0229others(1): Show | 4 | HG02055.hp1 HG02572.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+592_783+607dup others(16): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(11): Show |
1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783+590_783+607dup others(18): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0235a0001c0003t0001g0022 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.783+589_783+607dup others(19): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0219 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.783+588_783+607dup others(20): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
A | ATTTTTTT others(21): Show |
1 | a0002c0002t0001g0270 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.783+580_783+607dup others(28): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
ATTT | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(2): Show | 6 | HG00735.hp2 HG01081.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+605_783+607del others(3): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
ATTTTTTT others(3): Show |
A | 13 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(10): Show | 13 | HG01928.hp2 HG01943.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.783+598_783+607del others(10): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182318
|
ATTTTTTT others(4): Show |
A | 1 | a0002c0002t0001g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.783+597_783+607del others(11): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182318 | |||||
chr4:168182382
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0229 | 3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.783+641G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182382 | ||||||
chr4:168182456
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.783+715A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182456 | ||||||
chr4:168182483
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.783+742A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182483 | ||||||
chr4:168182485
|
C | CCCCCCCC others(36): Show |
1 | a0001c0001t0001g0069 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.783+744_783+745ins others(43): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182485 | ||||||
chr4:168182486
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.783+745A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182486 | ||||||
chr4:168182534
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.783+793T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182534 | ||||||
chr4:168182541
|
C | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.783+800C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182541 | ||||||
chr4:168182544
|
A | G | 1 | a0002c0012t0001g0113 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783+803A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182544 | ||||||
chr4:168182623
|
G | A | 14 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(11): Show | 14 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.783+882G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182623 | ||||||
chr4:168182625
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.783+884G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182625 | ||||||
chr4:168182882
|
C | A | 1 | a0002c0002t0001g0254 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.783+1141C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182882 | ||||||
chr4:168182883
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(94): Show | 100 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.783+1142A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182883 | ||||||
chr4:168182978
|
C | A | 1 | a0002c0002t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.783+1237C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168182978 | ||||||
chr4:168182983
|
T | TG | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.783+1244dupG | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168182983 | |||||
chr4:168183009
|
G | GA | 24 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0079others(21): Show | 24 | HG01243.hp1 HG01496.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.783+1288dupA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168183009 | |||||
chr4:168183009
|
GA | G | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0106others(11): Show | 14 | HG00639.hp1 HG01109.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.783+1288delA | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168183009 | |||||
chr4:168183009
|
GAAAAAA | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 6 | HG01123.hp2 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+1283_783+1288d others(8): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168183009 | |||||
chr4:168183009
|
GAAAAAAA | G | 50 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0009others(47): Show | 52 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.783+1282_783+1288d others(9): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 168183009 | |||||
chr4:168183024
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.783+1283A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183024 | ||||||
chr4:168183175
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 8 | HG02258.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1384T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183175 | ||||||
chr4:168183497
|
T | C | 2 | a0002c0002t0001g0102a0002c0002t0001g0103 | 2 | HG01069.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.784-1062T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183497 | ||||||
chr4:168183688
|
T | G | 1 | a0002c0002t0001g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.784-871T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183688 | ||||||
chr4:168183828
|
T | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 54 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.784-731T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183828 | ||||||
chr4:168183840
|
T | C | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(29): Show | 32 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-719T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183840 | ||||||
chr4:168183849
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-710T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168183849 | ||||||
chr4:168184002
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | HG02451.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-557C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168184002 | ||||||
chr4:168184018
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.784-541G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168184018 | ||||||
chr4:168184226
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0232a0002c0002t0001g0274others(1): Show | 5 | HG02280.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-333T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168184226 | ||||||
chr4:168184412
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 90 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.784-147A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168184412 | ||||||
chr4:168184529
|
T | G | 1 | a0002c0002t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.784-30T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 10/11 | chr4 | 168184529 | ||||||
chr4:168184782
|
G | A | 1 | a0002c0002t0001g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.906+101G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168184782 | ||||||
chr4:168184870
|
C | T | 1 | a0002c0002t0001g0134 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.906+189C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168184870 | ||||||
chr4:168185026
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.906+345C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168185026 | ||||||
chr4:168185243
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0052others(38): Show | 42 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.906+562G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168185243 | ||||||
chr4:168185342
|
T | C | 24 | a0001c0003t0001g0013a0001c0003t0001g0016a0001c0003t0001g0020others(21): Show | 24 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.906+661T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168185342 | ||||||
chr4:168185721
|
C | G | 4 | a0003c0004t0001g0096a0003c0004t0001g0220a0003c0004t0001g0223others(1): Show | 4 | HG02717.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1040C>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168185721 | ||||||
chr4:168185736
|
A | G | 14 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(11): Show | 14 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.906+1055A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168185736 | ||||||
chr4:168186019
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.906+1338T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186019 | ||||||
chr4:168186061
|
T | C | 42 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0009others(39): Show | 44 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.907-1305T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186061 | ||||||
chr4:168186091
|
A | C | 1 | a0002c0002t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.907-1275A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186091 | ||||||
chr4:168186235
|
T | G | 1 | a0002c0002t0001g0063 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.907-1131T>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186235 | ||||||
chr4:168186271
|
A | T | 1 | a0001c0003t0001g0021 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.907-1095A>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186271 | ||||||
chr4:168186291
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 54 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.907-1075C>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186291 | ||||||
chr4:168186458
|
T | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 54 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.907-908T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186458 | ||||||
chr4:168186601
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 58 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.907-765T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186601 | ||||||
chr4:168186838
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.907-528T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168186838 | ||||||
chr4:168187050
|
A | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0198others(31): Show | 35 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.907-316A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187050 | ||||||
chr4:168187055
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0092 | 2 | NA18968.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.907-311A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187055 | ||||||
chr4:168187069
|
T | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(48): Show | 54 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.907-297T>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187069 | ||||||
chr4:168187138
|
G | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(29): Show | 32 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.907-228G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187138 | ||||||
chr4:168187146
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.907-220G>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187146 | ||||||
chr4:168187181
|
A | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.907-185A>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187181 | ||||||
chr4:168187199
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0228 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.907-167T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187199 | ||||||
chr4:168187221
|
G | T | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(29): Show | 32 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.907-145G>T | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187221 | ||||||
chr4:168187247
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0010others(4): Show | 8 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.907-119A>G | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187247 | ||||||
chr4:168187321
|
C | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(29): Show | 32 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.907-45C>A | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187321 | ||||||
chr4:168187349
|
T | C | 14 | a0002c0002t0001g0143a0002c0002t0001g0146a0002c0002t0001g0153others(11): Show | 14 | HG01496.hp2 HG01928.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.907-17T>C | ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 11/11 | chr4 | 168187349 |