Variant #0001002493 (NC_000016.9:g.67977914G>A, NM_000229.1:c.91C>T (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.67977914G>A
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.91C>T (p.L31F), SLC12A4(NM_005072.5):c.*829C>T
ISCN -
DB-ID LCAT_000245
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LCAT NM_000229.1 ?/. - c.91C>T r.(?) p.(Leu31Phe)
SLC12A4 NM_005072.4 ?/. - c.*829C>T r.(=) p.(=)


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