Variant #0000854838 (NC_000017.10:g.3386820G>A, NM_000049.2:c.460G>A (ASPA))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3386820G>A
DNA change (hg38) -
Published as ASPA(NM_000049.3):c.460G>A (p.V154I)
ISCN -
DB-ID ASPA_018116
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
ASPA NM_000049.2 ?/. - c.460G>A r.(?) p.(Val154Ile)
TRPV3 NM_145068.3 ?/. - c.*30391C>T r.(=) p.(=)


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