Variant #0000617282 (NC_000019.9:g.1037809_1037810del, NM_019112.3:c.-2524_-2523del (ABCA7))

Chromosome 19
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.1037809_1037810del
DNA change (hg38) g.1037810_1037811del
Published as CNN2(NM_004368.2):c.840_841del (p.(Asp281TrpfsTer17))
ISCN -
DB-ID ABCA7_000036
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-15 09:24:09 +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.840_841del r.(?) p.(Asp281TrpfsTer17)
ABCA7 NM_019112.3 ?/. - c.-2524_-2523del r.(?) p.(=)


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