Variant #0000326017 (NC_000019.9:g.1037828A>G, NM_019112.3:c.-2505A>G (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.1037828A>G
DNA change (hg38) g.1037829A>G
Published as CNN2(NM_004368.2):c.859A>G (p.(Thr287Ala))
ISCN -
DB-ID CNN2_000006
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 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     
CNN2 NM_004368.2 -?/. - c.859A>G r.(?) p.(Thr287Ala)
ABCA7 NM_019112.3 -?/. - c.-2505A>G r.(?) p.(=)


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