Variant #0000854587 (NC_000016.9:g.67973896C>T, NM_000229.1:c.1234G>A (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.67973896C>T
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.1234G>A (p.E412K)
ISCN -
DB-ID LCAT_000204
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) 2.0E-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 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.1234G>A r.(?) p.(Glu412Lys)
PSMB10 NM_002801.3 ?/. - c.-3244G>A r.(?) p.(=)
SLC12A4 NM_005072.4 ?/. - c.*4847G>A r.(=) p.(=)


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