Variant #0000246696 (NC_000008.10:g.62577831A>G, NC_000008.10(NM_004318.3):c.323-11612T>C (ASPH))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62577831A>G
DNA change (hg38) g.61665272A>G
Published as ASPH(NM_020164.4):c.657T>C (p.N219=), ASPH(NM_020164.5):c.657T>C (p.N219=)
ISCN -
DB-ID ASPH_000007 See all 2 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) 0.00197 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.323-11612T>C r.(=) p.(=)
CLVS1 NM_173519.2 -/. - c.*165730A>G r.(=) p.(=)


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