Variant #0000678417 (NC_000008.10:g.62559353A>G, NM_004318.3:c.575T>C (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.62559353A>G
DNA change (hg38) -
Published as ASPH(NM_004318.3):c.575T>C (p.V192A)
ISCN -
DB-ID ASPH_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.575T>C r.(?) p.(Val192Ala)
CLVS1 NM_173519.2 -?/. - c.*147252A>G r.(=) p.(=)


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