Variant #0000535190 (NC_000008.10:g.62550937dup, NC_000008.10(NM_004318.3):c.791-3dup (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.62550937dup
DNA change (hg38) g.61638378dup
Published as ASPH(NM_001164750.1):c.704-3dup (p.?), ASPH(NM_004318.4):c.791-3dupT
ISCN -
DB-ID ASPH_000028 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) 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 2023-01-11 15:44:22 +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.791-3dup r.spl? p.?
CLVS1 NM_173519.2 -?/. - c.*138836dup r.(?) p.(=)


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