Variant #0000254184 (NC_000008.10:g.62580819A>T, NC_000008.10(NM_004318.3):c.322+12708T>A (ASPH))

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.62580819A>T
DNA change (hg38) g.61668260A>T
Published as ASPH(NM_020164.4):c.296T>A (p.V99E), ASPH(NM_020164.5):c.296T>A (p.V99E, p.(Val99Glu))
ISCN -
DB-ID ASPH_000010 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) 0.00034 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPH NM_004318.3 -?/. - c.322+12708T>A r.(=) p.(=)
CLVS1 NM_173519.2 -?/. - c.*168718A>T r.(=) p.(=)


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