Variant #0000678366 (NC_000008.10:g.21904138C>T, NM_003867.2:c.351C>T (FGF17))

Chromosome 8
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.21904138C>T
DNA change (hg38) -
Published as FGF17(NM_003867.3):c.351C>T (p.I117=)
ISCN -
DB-ID EPB49_000003
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPB49 NM_001978.2 -?/. - c.-13041C>T r.(?) p.(=)
FGF17 NM_003867.2 -?/. - c.351C>T r.(?) p.(Ile117=)


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