Variant #0000522192 (NC_000004.11:g.1808989A>C, NM_000142.4:c.2421A>C (FGFR3))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1808989A>C
DNA change (hg38) g.1807262A>C
Published as -
ISCN -
DB-ID LETM1_000010
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 11:03:41 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR3 NM_000142.4 +/. - c.2421A>C r.(?) p.(Ter807CysextTer101)
LETM1 NM_012318.2 +/. - c.*7162T>G r.(=) p.(=)


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