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 |
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
Descrption | Source | Links |
---|---|---|
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