Variant #0001014218 (NC_000006.11:g.42932564C>A, NM_000287.3:c.2770G>T (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.42932564C>A
DNA change (hg38) -
Published as PEX6(NM_000287.3):c.2770G>T (p.A924S), PEX6(NM_000287.4):c.2770G>T (p.A924S)
ISCN -
DB-ID PEX6_000129 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) 0.00147 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 -?/. - c.2770G>T r.(?) p.(Ala924Ser)
CNPY3 NM_006586.3 -?/. - c.*26035C>A r.(=) p.(=)
GNMT NM_018960.4 -?/. - c.*1120C>A r.(=) p.(=)


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