Variant #0000326019 (NC_000019.9:g.1037856T>C, NM_019112.3:c.-2477T>C (ABCA7))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1037856T>C
DNA change (hg38) g.1037857T>C
Published as CNN2(NM_004368.2):c.887T>C (p.(Val296Ala))
ISCN -
DB-ID CNN2_000008
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNN2 NM_004368.2 -?/. - c.887T>C r.(?) p.(Val296Ala)
ABCA7 NM_019112.3 -?/. - c.-2477T>C r.(?) p.(=)


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