Variant #0000535188 (NC_000008.10:g.62550925A>G, NC_000008.10(NM_004318.3):c.791-3T>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.62550925A>G
DNA change (hg38) g.61638366A>G
Published as ASPH(NM_001164750.1):c.704-3T>C (p.?)
ISCN -
DB-ID ASPH_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 20:13:17 +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.791-3T>C r.spl? p.?
CLVS1 NM_173519.2 -?/. - c.*138824A>G r.(=) p.(=)


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