chr10:51568377:A>C Detail (hg19) (NCOA4)

Information

Genome

Assembly Position
hg19 chr10:51,568,377-51,568,377
hg38 chr10:46,027,444-46,027,444 

HGVS

Type Transcript Protein
RefSeq NM_001145260.1:c.21A>C NP_001138732.1:p.Thr7=
NM_001145261.1:c.-15+3081A>C
NM_001145263.1:c.-15+3081A>C
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601984 OMIM
HGNC 7671 HGNC
Ensembl ENSG00000266412 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant 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
0.256 Malignant neoplasm of prostate Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4,... BeFree 20717903 Detail
0.003 prostate carcinoma Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4,... BeFree 20717903 Detail
0.005 Malignant neoplasm of prostate Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4,... BeFree 20717903 Detail
0.011 prostate carcinoma Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4,... BeFree 20717903 Detail
Annotation

Annotations

DescrptionSourceLinks
Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been... DisGeNET Detail
Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been... DisGeNET Detail
Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been... DisGeNET Detail
Of note, rs7000448 is in strong linkage disequilibrium with rs10761581 in NCOA4, a SNP that has been... 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
rs10761581 dbSNP
Genome
hg19
Position
chr10:51,568,377-51,568,377
Variant Type
snv
Reference Allele
A
Alternative Allele
C
Genome browser