Variant #0000883215 (NC_000001.10:g.231402097_231402104dup, NM_014236.3:c.999_1006dup (GNPAT))

Chromosome 1
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.231402097_231402104dup
DNA change (hg38) -
Published as GNPAT(NM_001316350.1):c.816_823dup (p.(Ser275TyrfsTer10))
ISCN -
DB-ID C1orf131_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNPAT NM_014236.3 ?/. - c.999_1006dup r.(?) p.(Ser336Tyrfs*10)
C1orf131 NM_152379.2 ?/. - c.-25217_-25210dup r.(?) p.(=)


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