Variant #0000994076 (NC_000004.11:g.123747943G>C, NM_002006.4:c.13G>C (FGF2))

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.123747943G>C
DNA change (hg38) -
Published as FGF2(NM_002006.4):c.13G>C (p.(Gly5Arg))
ISCN -
DB-ID FGF2_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) 0.0003 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGF2 NM_002006.4 -?/. - c.13G>C r.(?) p.(Gly5Arg)
NUDT6 NM_007083.4 -?/. - c.*66040C>G r.(=) p.(=)


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