chr19:13365335:A>G Detail (hg38) (CACNA1A)

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

Genome

Assembly	Position
hg19	chr19:13,476,149-13,476,149 View the variant detail on this assembly version.
hg38	chr19:13,365,335-13,365,335

HGVS

CACNA1A

Type	Transcript	Protein
RefSeq	NM_001127222.1:c.766T>C	NP_001120694.1:p.Cys256Arg
	NM_000068.3:c.766T>C	NP_000059.3:p.Cys256Arg
	NM_001174080.1:c.766T>C	NP_001167551.1:p.Cys256Arg
	NM_001127221.1:c.766T>C	NP_001120693.1:p.Cys256Arg
	NM_023035.2:c.766T>C	NP_075461.2:p.Cys256Arg
Ensemble	ENST00000360228.11:c.766T>C	ENST00000360228.11:p.Cys256Arg
	ENST00000573710.7:c.766T>C	ENST00000573710.7:p.Cys256Arg
	ENST00000585802.7:c.766T>C	ENST00000585802.7:p.Cys256Arg
	ENST00000587525.6:c.766T>C	ENST00000587525.6:p.Cys256Arg
	ENST00000635727.1:c.766T>C	ENST00000635727.1:p.Cys256Arg
	ENST00000635895.1:c.766T>C	ENST00000635895.1:p.Cys256Arg
	ENST00000636012.1:c.766T>C	ENST00000636012.1:p.Cys256Arg
	ENST00000636389.1:c.766T>C	ENST00000636389.1:p.Cys256Arg
	ENST00000636473.2:c.766T>C	ENST00000636473.2:p.Cys256Arg
	ENST00000636549.1:c.766T>C	ENST00000636549.1:p.Cys256Arg
	ENST00000637276.1:c.766T>C	ENST00000637276.1:p.Cys256Arg
	ENST00000637432.1:c.766T>C	ENST00000637432.1:p.Cys256Arg
	ENST00000637736.1:c.625T>C	ENST00000637736.1:p.Cys209Arg
	ENST00000637769.1:c.766T>C	ENST00000637769.1:p.Cys256Arg
	ENST00000637819.2:c.766T>C	ENST00000637819.2:p.Cys256Arg
	ENST00000637927.1:c.766T>C	ENST00000637927.1:p.Cys256Arg
	ENST00000638009.2:c.766T>C	ENST00000638009.2:p.Cys256Arg
	ENST00000638029.1:c.766T>C	ENST00000638029.1:p.Cys256Arg
	ENST00000664864.1:c.961T>C	ENST00000664864.1:p.Cys321Arg

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	not provided
Review star
Show details

Links

CACNA1A

Type	Database	ID	Link
Gene	MIM	601011	OMIM
	HGNC	1388	HGNC
	Ensembl	ENSG00000141837	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

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
not provided		no assertion provided	episodic ataxia type 2	not provided	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.575	Episodic ataxia type 2 (disorder)	Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 c...	UNIPROT	15173248	Detail

Annotation

Annotations

Descrption	Source	Links
NM_001127222.2(CACNA1A):c.766T>C (p.Cys256Arg) AND Episodic ataxia type 2	ClinVar	Detail
Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic atax...	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: rs121908231 dbSNP
Genome: hg38
Position: chr19:13,365,335-13,365,335
Variant Type: snv
Reference Allele: A
Alternative Allele: G

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