Variant #0000528876 (NC_000006.11:g.42936151C>G, NM_000287.3:c.1565G>C (PEX6))

Chromosome 6
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.42936151C>G
DNA change (hg38) g.42968413C>G
Published as PEX6(NM_000287.3):c.1565G>C (p.R522P), PEX6(NM_000287.4):c.1565G>C (p.(Arg522Pro), p.R522P)
ISCN -
DB-ID CNPY3_000003 See all 3 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) 2.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
PEX6 NM_000287.3 ?/. - c.1565G>C r.(?) p.(Arg522Pro)
CNPY3 NM_006586.3 ?/. - c.*29622C>G r.(=) p.(=)
GNMT NM_018960.4 ?/. - c.*4707C>G r.(=) p.(=)


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