Variant #0000984390 (NC_000023.10:g.110406196_110406198del, NM_002578.3:c.522_524del (PAK3))

Chromosome X
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.110406196_110406198del
DNA change (hg38) -
Published as PAK3(NM_002578.5):c.522_524delAGA (p.E174del)
ISCN -
DB-ID PAK3_000084
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +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     
PAK3 NM_001128166.1 ?/. - c.522_524del r.(?) p.(Glu174del)
PAK3 NM_002578.3 ?/. - c.522_524del r.(?) p.(Glu174del)


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