Variant #0000538940 (NC_000010.10:g.103541595A>T, NM_033163.3:c.-5938T>A (FGF8))

Chromosome 10
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.103541595A>T
DNA change (hg38) g.101781838A>T
Published as NPM3(NM_006993.2):c.435T>A (p.(Asp145Glu))
ISCN -
DB-ID FGF8_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) 0.00026 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 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NPM3 NM_006993.2 -?/. - c.435T>A r.(?) p.(Asp145Glu)
MGEA5 NM_012215.3 -?/. - c.*4613T>A r.(=) p.(=)
FGF8 NM_033163.3 -?/. - c.-5938T>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.