Variant #0000331024 (NC_000006.11:g.42932080G>A, NM_000287.3:c.2936C>T (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.42932080G>A
DNA change (hg38) g.42964342G>A
Published as PEX6(NM_000287.3):c.2936C>T (p.(Ala979Val))
ISCN -
DB-ID PEX6_000126 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) 0.00185 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX6 NM_000287.3 ?/. - c.2936C>T r.(?) p.(Ala979Val)
CNPY3 NM_006586.3 ?/. - c.*25551G>A r.(=) p.(=)
GNMT NM_018960.4 ?/. - c.*636G>A r.(=) p.(=)


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