Variant #0000887256 (NC_000006.11:g.42933047A>G, NM_000287.3:c.2531T>C (PEX6))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42933047A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CNPY3_000019
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) 0.00076 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 -/. - c.2531T>C r.(?) p.(Val844Ala)
CNPY3 NM_006586.3 -/. - c.*26518A>G r.(=) p.(=)
GNMT NM_018960.4 -/. - c.*1603A>G r.(=) p.(=)


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