Variant #0000276993 (NC_000016.9:g.81391507C>T, NM_022041.3:c.944C>T (GAN))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.81391507C>T
DNA change (hg38) g.81357902C>T
Published as GAN(NM_022041.3):c.944C>T (p.P315L), GAN(NM_022041.4):c.944C>T (p.P315L, p.(Pro315Leu))
ISCN -
DB-ID GAN_000042 See all 4 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) 0.00015 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAN NM_022041.3 +/. - c.944C>T r.(?) p.(Pro315Leu)


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