Variant #0000542398 (NC_000011.9:g.116661777C>G, NM_001166598.1:c.168G>C (APOA5))

Chromosome 11
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.116661777C>G
DNA change (hg38) g.116791061C>G
Published as APOA5(NM_052968.5):c.168G>C (p.L56=)
ISCN -
DB-ID APOA5_000051
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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOA5 NM_001166598.1 -?/. - c.168G>C r.(?) p.(Leu56=)
ZNF259 NM_003904.3 -?/. - c.-3071G>C r.(?) p.(=)


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