Variant #0000886214 (NC_000004.11:g.1808930G>A, NM_000142.4:c.2362G>A (FGFR3))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1808930G>A
DNA change (hg38) -
Published as FGFR3(NM_000142.4):c.2362G>A (p.(Val788Met))
ISCN -
DB-ID LETM1_000029 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR3 NM_000142.4 ?/. - c.2362G>A r.(?) p.(Val788Met)
LETM1 NM_012318.2 ?/. - c.*7221C>T r.(=) p.(=)


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