Variant #0000981997 (NC_000016.9:g.67974058T>C, NM_000229.1:c.1072A>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.67974058T>C
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.1072A>G (p.T358A)
ISCN -
DB-ID LCAT_000240
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 2024-04-19 20:27:30 +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.1072A>G r.(?) p.(Thr358Ala)
PSMB10 NM_002801.3 ?/. - c.-3406A>G r.(?) p.(=)
SLC12A4 NM_005072.4 ?/. - c.*4685A>G r.(=) p.(=)


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