Variant #0000522190 (NC_000004.11:g.1808899C>T, NM_000142.4:c.2331C>T (FGFR3))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1808899C>T
DNA change (hg38) g.1807172C>T
Published as FGFR3(NM_000142.4):c.2331C>T (p.(Thr777=))
ISCN -
DB-ID LETM1_000008
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) 0.00017 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGFR3 NM_000142.4 -?/. - c.2331C>T r.(?) p.(Thr777=)
LETM1 NM_012318.2 -?/. - c.*7252G>A r.(=) p.(=)


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