chr15:42693961:C>T Detail (hg19) (CAPN3)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr15:42,693,961-42,693,961
hg38	chr15:42,401,763-42,401,763 View the variant detail on this assembly version.

HGVS

CAPN3

Type	Transcript	Protein
RefSeq	NM_173087.1:c.1333C>T	NP_775110.1:p.Arg445Trp
	NM_024344.1:c.1477C>T	NP_077320.1:p.Arg493Trp
	NM_000070.2:c.1477C>T	NP_000061.1:p.Arg493Trp
Ensemble	ENST00000349748.8:c.1333C>T	ENST00000349748.8:p.Arg445Trp
	ENST00000357568.8:c.1477C>T	ENST00000357568.8:p.Arg493Trp
	ENST00000318023.11:c.1333C>T	ENST00000318023.11:p.Arg445Trp
	ENST00000397163.8:c.1477C>T	ENST00000397163.8:p.Arg493Trp

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

JP	HGVD:[No Data.]
	ToMMo:[No Data.]
	NCBN:[No Data.]
	NCBN(Hondo):[No Data.]
	NCBN(Ryukyu):[No Data.]
East asia	ExAC:<0.001

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
Review star
Show details

Links

CAPN3

Type	Database	ID	Link
Gene	MIM	114240	OMIM
	HGNC	1480	HGNC
	Ensembl	ENSG00000092529	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM961724	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic Likely pathogenic	2022-08-02	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Pathogenic Likely pathogenic	2024-01-12	criteria provided, multiple submitters, no conflicts	autosomal recessive limb-girdle muscular dystrophy type 2A	germline unknown	Detail
Pathogenic	2023-06-15	criteria provided, single submitter	Muscular dystrophy, limb-girdle, autosomal dominant 4	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.573	Limb-girdle muscular dystrophy type 2A	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000070.3(CAPN3):c.1477C>T (p.Arg493Trp) AND not provided	ClinVar	Detail
NM_000070.3(CAPN3):c.1477C>T (p.Arg493Trp) AND Autosomal recessive limb-girdle muscular dystrophy ty...	ClinVar	Detail
NM_000070.3(CAPN3):c.1477C>T (p.Arg493Trp) AND Muscular dystrophy, limb-girdle, autosomal dominant 4	ClinVar	Detail
NA	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: rs557164942 dbSNP
Genome: hg19
Position: chr15:42,693,961-42,693,961
Variant Type: snv
Reference Allele: C
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8238
East Asian Allele Counts (ExAC): 0
East Asian Heterozygous Counts (ExAC): 0
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 0.0
Chromosome Counts in All Race (ExAC): 116610
Allele Counts in All Race (ExAC): 2
Heterozygous Counts in All Race (ExAC): 2
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 1.715118771974959E-5

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