Variant #0000978149 (NC_000008.10:g.17924719T>C, NC_000008.10(NM_004315.4):c.430+10A>G (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.17924719T>C
DNA change (hg38) -
Published as ASAH1(NM_004315.6):c.430+10A>G, ASAH1(NM_177924.5):c.382+10A>G
ISCN -
DB-ID ASAH1_000035 See all 3 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) 0.00053 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 2024-04-19 20:27:30 +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     
ASAH1 NM_004315.4 -?/. - c.430+10A>G r.(=) p.(=)


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