Variant #0000926328 (NC_000016.9:g.67976634T>C, NM_000229.1:c.463A>G (LCAT))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67976634T>C
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.463A>G (p.N155D)
ISCN -
DB-ID LCAT_000196 See all 2 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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.463A>G r.(?) p.(Asn155Asp)
SLC12A4 NM_005072.4 +/. - c.*2109A>G r.(=) p.(=)


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