chr19:43575535:G>A Detail (hg38) (XRCC1)

Information

Genome

Assembly Position
hg19 chr19:44,079,687-44,079,687 View the variant detail on this assembly version.
hg38 chr19:43,575,535-43,575,535

HGVS

Type Transcript Protein
RefSeq NM_006297.2:c.-77C>T
Ensemble ENST00000543982.5:c.-77C>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.895
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.895

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 194360 OMIM
HGNC 12828 HGNC
Ensembl ENSG00000073050 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv62218104 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.012 Non-small cell lung carcinoma This study tested whether XPD Lys751Gln and XRCC1 T-77C polymorphisms were assoc... BeFree 21129812 Detail
0.005 Non-small cell lung carcinoma This study tested whether XPD Lys751Gln and XRCC1 T-77C polymorphisms were assoc... BeFree 21129812 Detail
0.012 Non-small cell lung carcinoma A novel T-77C polymorphism in DNA repair gene XRCC1 contributes to diminished pr... BeFree 16652158 Detail
0.012 Non-small cell lung carcinoma Our results suggest that XRCC1 T-77C variants (TC + CC) may act as a favorable p... BeFree 19052039 Detail
0.020 Carcinoma of lung Thus, there is a significant association of XRCC1 rs3213245 polymorphism with lu... BeFree 24470137 Detail
0.100 Malignant neoplasm of lung Thus, there is a significant association of XRCC1 rs3213245 polymorphism with lu... BeFree 24470137 Detail
0.006 Paroxysmal atrial tachycardia No associations with lung cancer risk were found for the XRCC1 -77 T/C, the XPA ... BeFree 17531525 Detail
0.123 Squamous cell carcinoma of esophagus Recently, we reported a SNP (rs3213245, -77T>C) in the XRCC1 gene 5' untransl... BeFree 16652158 Detail
<0.001 Squamous cell carcinoma of esophagus In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala a... BeFree 15205355 Detail
<0.001 Squamous cell carcinoma of esophagus In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala a... BeFree 15205355 Detail
<0.001 Squamous cell carcinoma of esophagus In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala a... BeFree 15205355 Detail
<0.001 Squamous cell carcinoma of esophagus In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala a... BeFree 15205355 Detail
0.123 Squamous cell carcinoma of esophagus In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala a... BeFree 15205355 Detail
Annotation

Annotations

DescrptionSourceLinks
This study tested whether XPD Lys751Gln and XRCC1 T-77C polymorphisms were associated with survival ... DisGeNET Detail
This study tested whether XPD Lys751Gln and XRCC1 T-77C polymorphisms were associated with survival ... DisGeNET Detail
A novel T-77C polymorphism in DNA repair gene XRCC1 contributes to diminished promoter activity and ... DisGeNET Detail
Our results suggest that XRCC1 T-77C variants (TC + CC) may act as a favorable prognostic indicator ... DisGeNET Detail
Thus, there is a significant association of XRCC1 rs3213245 polymorphism with lung cancer risk. DisGeNET Detail
Thus, there is a significant association of XRCC1 rs3213245 polymorphism with lung cancer risk. DisGeNET Detail
No associations with lung cancer risk were found for the XRCC1 -77 T/C, the XPA -4 G/A and the XPC P... DisGeNET Detail
Recently, we reported a SNP (rs3213245, -77T&gt;C) in the XRCC1 gene 5' untranslated region (UTR) wa... DisGeNET Detail
In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala and MBD4 Glu346Lys) a... DisGeNET Detail
In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala and MBD4 Glu346Lys) a... DisGeNET Detail
In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala and MBD4 Glu346Lys) a... DisGeNET Detail
In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala and MBD4 Glu346Lys) a... DisGeNET Detail
In the final model, 4 SNPs, including 2 in the coding regions (ADPRT Val762Ala and MBD4 Glu346Lys) a... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs3213245 dbSNP
Genome
hg38
Position
chr19:43,575,535-43,575,535
Variant Type
snv
Reference Allele
G
Alternative Allele
A
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs3213245
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.8952
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
15003
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
East Asian Chromosome Counts (ExAC)
6558
East Asian Allele Counts (ExAC)
5867
East Asian Heterozygous Counts (ExAC)
647
East Asian Homozygous Counts (ExAC)
2610
East Asian Allele Frequency (ExAC)
0.8946325099115584
Chromosome Counts in All Race (ExAC)
85302
Allele Counts in All Race (ExAC)
56260
Heterozygous Counts in All Race (ExAC)
19638
Homozygous Counts in All Race (ExAC)
18311
Allele Frequency in All Race (ExAC)
0.6595390494947363
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