chr2:240786339:C>G Detail (hg38) (KIF1A)

Go to:

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

Information

Genome

Assembly	Position
hg19	chr2:241,725,756-241,725,756 View the variant detail on this assembly version.
hg38	chr2:240,786,339-240,786,339

HGVS

KIF1A

Type	Transcript	Protein
RefSeq	NM_004321.6:c.604G>C	NP_004312.2:p.Ala202Pro
	NM_001244008.1:c.604G>C	NP_001230937.1:p.Ala202Pro
	NM_001320705.1:c.604G>C	NP_001307634.1:p.Ala202Pro
Ensemble	ENST00000320389.12:c.604G>C	ENST00000320389.12:p.Ala202Pro
	ENST00000404283.9:c.604G>C	ENST00000404283.9:p.Ala202Pro
	ENST00000431776.7:c.604G>C	ENST00000431776.7:p.Ala202Pro
	ENST00000498729.9:c.604G>C	ENST00000498729.9:p.Ala202Pro
	ENST00000647572.2:c.604G>C	ENST00000647572.2:p.Ala202Pro
	ENST00000647731.1:c.604G>C	ENST00000647731.1:p.Ala202Pro
	ENST00000647885.1:c.604G>C	ENST00000647885.1:p.Ala202Pro
	ENST00000648047.2:c.604G>C	ENST00000648047.2:p.Ala202Pro
	ENST00000648129.1:c.604G>C	ENST00000648129.1:p.Ala202Pro
	ENST00000648364.1:c.604G>C	ENST00000648364.1:p.Ala202Pro
	ENST00000648680.1:c.604G>C	ENST00000648680.1:p.Ala202Pro
	ENST00000649096.1:c.604G>C	ENST00000649096.1:p.Ala202Pro
	ENST00000649306.1:c.604G>C	ENST00000649306.1:p.Ala202Pro
	ENST00000650053.1:c.604G>C	ENST00000650053.1:p.Ala202Pro
	ENST00000650130.1:c.604G>C	ENST00000650130.1:p.Ala202Pro
	ENST00000674907.2:c.604G>C	ENST00000674907.2:p.Ala202Pro
	ENST00000675126.2:c.604G>C	ENST00000675126.2:p.Ala202Pro
	ENST00000675940.2:c.604G>C	ENST00000675940.2:p.Ala202Pro
	ENST00000715177.1:c.604G>C	ENST00000715177.1:p.Ala202Pro

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely pathogenic
Review star
Show details

Links

KIF1A

Type	Database	ID	Link
Gene	MIM	601255	OMIM
	HGNC	888	HGNC
	Ensembl	ENSG00000130294	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
Likely pathogenic	2020-06-15	criteria provided, single submitter	Intellectual disability, autosomal dominant 9	de novo germline unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.240	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_001244008.2(KIF1A):c.604G>C (p.Ala202Pro) AND Intellectual disability, autosomal dominant 9	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: rs672601366 dbSNP
Genome: hg38
Position: chr2:240,786,339-240,786,339
Variant Type: snv
Reference Allele: C
Alternative Allele: G

Genome browser