chr4:1803744:A>T Detail (hg38) (FGFR3)

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

Genome

Assembly	Position
hg19	chr4:1,805,471-1,805,471 View the variant detail on this assembly version.
hg38	chr4:1,803,744-1,803,744

HGVS

FGFR3

Type	Transcript	Protein
RefSeq	NM_001163213.1:c.1082-586A>T
	NM_022965.3:c.971A>T	NP_075254.1:p.Asn324Ile
	NM_000142.4:c.983A>T	NP_000133.1:p.Asn328Ile
Ensemble	ENST00000340107.9:c.1082-586A>T
	ENST00000352904.6:c.931-1080A>T
	ENST00000412135.7:c.971A>T	ENST00000412135.7:p.Asn324Ile
	ENST00000440486.8:c.983A>T	ENST00000440486.8:p.Asn328Ile
	ENST00000481110.7:c.983A>T	ENST00000481110.7:p.Asn328Ile

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

FGFR3

Type	Database	ID	Link
Gene	MIM	134934	OMIM
	HGNC	3690	HGNC
	Ensembl	ENSG00000068078	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	2019-11-30	criteria provided, single submitter	not provided	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.495	Hypochondroplasia (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000142.5(FGFR3):c.983A>T (p.Asn328Ile) AND not provided	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: rs587778817 dbSNP
Genome: hg38
Position: chr4:1,803,744-1,803,744
Variant Type: snv
Reference Allele: A
Alternative Allele: T

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