Variant #0000518768 (NC_000003.11:g.191888452G>A, NC_000003.11(NM_021032.4):c.415-7C>T (FGF12))

Chromosome 3
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.191888452G>A
DNA change (hg38) g.192170663G>A
Published as FGF12(NM_004113.5):c.229-7C>T (p.(=)), FGF12(NM_021032.4):c.415-9_415-7delTTCinsTTT
ISCN -
DB-ID FGF12_000003 See all 2 reported entries
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_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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGF12 NM_021032.4 -?/. - c.415-7C>T r.(=) p.(=)


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