Variant #0001054700 (NC_000013.10:g.100809544C>A, NM_000282.3:c.418C>A (PCCA))

Chromosome 13
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.100809544C>A
DNA change (hg38) -
Published as PCCA(NM_000282.4):c.418C>A (p.(His140Asn))
ISCN -
DB-ID A2LD1_000045
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCCA NM_000282.3 ?/. - c.418C>A r.(?) p.(His140Asn)
A2LD1 NM_001195087.1 ?/. - c.*374840G>T r.(=) p.(=)


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