Variant #0000887255 (NC_000006.11:g.42905443C>T, NM_000287.3:c.*26630G>A (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.42905443C>T
DNA change (hg38) -
Published as CNPY3(NM_006586.5):c.373-12C>T
ISCN -
DB-ID CNPY3_000018
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) 0.00371 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.*26630G>A r.(=) p.(=)
CNPY3 NM_006586.3 -?/. - c.373-12C>T r.(=) p.(=)
GNMT NM_018960.4 -?/. - c.-23063C>T r.(?) p.(=)


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