Variant #0000720942 (NC_000006.11:g.42937685C>T, NM_000287.3:c.1171G>A (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.42937685C>T
DNA change (hg38) -
Published as PEX6(NM_000287.3):c.1171G>A (p.E391K)
ISCN -
DB-ID GNMT_000002
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) 0.00041 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.1171G>A r.(?) p.(Glu391Lys)
GNMT NM_018960.4 ?/. - c.*6241C>T r.(=) p.(=)


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