Variant #0000534404 (NC_000008.10:g.17924613_17924614insTTTG, NC_000008.10(NM_004315.4):c.430+115_430+116insCAAA (ASAH1))

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.17924613_17924614insTTTG
DNA change (hg38) g.18067104_18067105insTTTG
Published as ASAH1(NM_004315.6):c.430+115_430+116insCAAA
ISCN -
DB-ID ASAH1_000050
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
ASAH1 NM_004315.4 -?/. - c.430+115_430+116insCAAA r.(=) p.(=)


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