Variant #0001027072 (NC_000017.10:g.78078895C>T, NM_000152.3:c.510C>T (GAA))

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.78078895C>T
DNA change (hg38) -
Published as GAA(NM_000152.3):c.510C>T (p.D170=), GAA(NM_000152.5):c.510C>T (p.D170=)
ISCN -
DB-ID GAA_000122 See all 6 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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GAA NM_000152.3 ?/. - c.510C>T r.(?) p.(Asp170=) -
CCDC40 NM_017950.3 ?/. - c.*5321C>T r.(=) p.(=) -


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