chr4:1805643:A>C Detail (hg38) (FGFR3)

Information

Genome

Assembly Position
hg19 chr4:1,807,370-1,807,370 View the variant detail on this assembly version.
hg38 chr4:1,805,643-1,805,643

HGVS

Type Transcript Protein
RefSeq NM_001163213.1:c.1625A>C NP_001156685.1:p.Asn542Thr
NM_022965.3:c.1607A>C NP_075254.1:p.Asn536Thr
NM_000142.4:c.1619A>C NP_000133.1:p.Asn540Thr
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic Likely pathogenic
Review star
Show details
Links
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 tgv194646117 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 1998-01-01 no assertion criteria provided hypochondroplasia germline Detail
Pathogenic Likely pathogenic 2022-03-17 criteria provided, multiple submitters, no conflicts not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.495 Hypochondroplasia (disorder) NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000142.5(FGFR3):c.1619A>C (p.Asn540Thr) AND Hypochondroplasia ClinVar Detail
NM_000142.5(FGFR3):c.1619A>C (p.Asn540Thr) 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
rs77722678 dbSNP
Genome
hg38
Position
chr4:1,805,643-1,805,643
Variant Type
snv
Reference Allele
A
Alternative Allele
C
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