Variant #0000851233 (NC_000006.11:g.42930887C>A, NM_000287.3:c.*1186G>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.42930887C>A
DNA change (hg38) -
Published as GNMT(NM_018960.5):c.529C>A (p.H177N)
ISCN -
DB-ID CNPY3_000013
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) 0.00042 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 2022-05-09 15:40:45 +02:00 (CEST)
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.*1186G>T r.(=) p.(=)
CNPY3 NM_006586.3 ?/. - c.*24358C>A r.(=) p.(=)
GNMT NM_018960.4 ?/. - c.529C>A r.(?) p.(His177Asn)


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