Variant #0000861271 (NC_000008.10:g.62559410del, NM_004318.3:c.518del (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.62559410del
DNA change (hg38) -
Published as ASPH(NM_001164750.1):c.431delA (p.(Asp144Valfs*20))
ISCN -
DB-ID ASPH_000057
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) 0.00126 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPH NM_004318.3 -?/. - c.518del r.(?) p.(Asp173Valfs*20)
CLVS1 NM_173519.2 -?/. - c.*147309del r.(?) p.(=)


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