Variant #0000866982 (NC_000023.10:g.110388143G>A, NC_000023.10(NM_002578.3):c.276+2719G>A (PAK3))

Chromosome X
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.110388143G>A
DNA change (hg38) -
Published as PAK3(NM_001128168.2):c.332G>A (p.G111E)
ISCN -
DB-ID PAK3_000077
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) 3.0E-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 16:01:56 +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.276+2719G>A r.(=) p.(=)
PAK3 NM_002578.3 -?/. - c.276+2719G>A r.(=) p.(=)


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