Variant #0000255016 (NC_000006.11:g.42936207A>G, NM_000287.3:c.1509T>C (PEX6))

Chromosome 6
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.42936207A>G
DNA change (hg38) g.42968469A>G
Published as PEX6(NM_000287.3):c.1509T>C (p.S503=)
ISCN -
DB-ID PEX6_000139
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 12:06:27 +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.1509T>C r.(?) p.(Ser503=)
CNPY3 NM_006586.3 -?/. - c.*29678A>G r.(=) p.(=)
GNMT NM_018960.4 -?/. - c.*4763A>G r.(=) p.(=)


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