Variant #0000549656 (NC_000013.10:g.101101497G>T, PCCA(NM_000282.3):c.1846-9G>T)

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.101101497G>T
DNA change (hg38) g.100449243G>T
Published as PCCA(NM_000282.3):c.1846-9G>T
ISCN -
DB-ID A2LD1_000013
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) 0.00158 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCCA NM_000282.3 -/. - c.1846-9G>T r.(=) p.(=)
A2LD1 NM_001195087.1 -/. - c.*82887C>A r.(=) p.(=)