Variant #0000854591 (NC_000016.9:g.67976633T>C, NM_000229.1:c.464A>G (LCAT))

Chromosome 16
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.67976633T>C
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.464A>G (p.N155S)
ISCN -
DB-ID LCAT_000209
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:47:41 +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     
LCAT NM_000229.1 ?/. - c.464A>G r.(?) p.(Asn155Ser)
SLC12A4 NM_005072.4 ?/. - c.*2110A>G r.(=) p.(=)


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