Variant #0000535196 (NC_000008.10:g.62580816_62580817insGTC, NC_000008.10(NM_004318.3):c.322+12710_322+12711insGAC (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.62580816_62580817insGTC
DNA change (hg38) g.61668257_61668258insGTC
Published as ASPH(NM_020164.4):c.298_299insGAC (p.A100delinsGP), ASPH(NM_020164.5):c.298_299insGAC (p.A100delinsGP)
ISCN -
DB-ID ASPH_000033 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) 0.0004 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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+12710_322+12711insGAC r.(=) p.(=)
CLVS1 NM_173519.2 -?/. - c.*168715_*168716insGTC r.(=) p.(=)


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