Variant #0001000390 (NC_000013.10:g.100921016A>G, NM_000282.3:c.893A>G (PCCA))

Chromosome 13
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.100921016A>G
DNA change (hg38) -
Published as PCCA(NM_000282.3):c.893A>G (p.(Lys298Arg))
ISCN -
DB-ID A2LD1_000043
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCCA NM_000282.3 +/. - c.893A>G r.(?) p.(Lys298Arg)
A2LD1 NM_001195087.1 +/. - c.*263368T>C r.(=) p.(=)


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