Variant #0000281102 (NC_000001.10:g.231406726dup, NM_014236.3:c.1502dup (GNPAT))

Chromosome 1
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.231406726dup
DNA change (hg38) g.231270980dup
Published as GNPAT(NM_014236.4):c.1502dupT (p.M501Ifs*19)
ISCN -
DB-ID GNPAT_000017
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPAT NM_014236.3 +/. - c.1502dup r.(?) p.(Met501IlefsTer19)
C1orf131 NM_152379.2 +/. - c.-29839dup r.(?) p.(=)


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