Variant #0000321356 (NC_000001.10:g.231402036C>G, NM_014236.3:c.938C>G (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.231402036C>G
DNA change (hg38) g.231266290C>G
Published as GNPAT(NM_014236.3):c.938C>G (p.(Ala313Gly))
ISCN -
DB-ID GNPAT_000014
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.938C>G r.(?) p.(Ala313Gly)
C1orf131 NM_152379.2 ?/. - c.-25149G>C r.(?) p.(=)


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