Variant #0000263034 (NC_000008.10:g.62580802T>C, NC_000008.10(NM_004318.3):c.322+12725A>G (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.62580802T>C
DNA change (hg38) g.61668243T>C
Published as ASPH(NM_020164.4):c.313A>G (p.K105E)
ISCN -
DB-ID ASPH_000009
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) 0.0004 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPH NM_004318.3 -?/. - c.322+12725A>G r.(=) p.(=)
CLVS1 NM_173519.2 -?/. - c.*168701T>C r.(=) p.(=)


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