Variant #0000296730 (NC_000023.10:g.110388083T>C, NC_000023.10(NM_002578.3):c.276+2659T>C (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.110388083T>C
DNA change (hg38) g.111144855T>C
Published as PAK3(NM_001128168.1):c.277-5T>C (p.?), PAK3(NM_002578.5):c.276+2659T>C
ISCN -
DB-ID PAK3_000044 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) 0.00422 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAK3 NM_001128166.1 -?/. - c.276+2659T>C r.(=) p.(=)
PAK3 NM_002578.3 -?/. - c.276+2659T>C r.(=) p.(=)


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