Variant #0000623307 (NC_000015.9:g.80473418_80473420del, NM_000137.2:c.1097_1099del (FAH))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.80473418_80473420del
DNA change (hg38) g.80181076_80181078del
Published as FAH(NM_000137.4):c.1097_1099delCGT (p.S366del)
ISCN -
DB-ID FAH_000043
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
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     
FAH NM_000137.2 +?/. - c.1097_1099del r.(?) p.(Ser366del)


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