Variant #0000864894 (NC_000016.9:g.67974757_67974758del, NC_000016.9(NM_000229.1):c.749-359_749-358del (LCAT))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67974757_67974758del
DNA change (hg38) -
Published as LCAT(NM_000229.2):c.749-359_749-358delTT
ISCN -
DB-ID LCAT_000206
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 16:01:56 +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.749-359_749-358del r.(=) p.(=)
PSMB10 NM_002801.3 -/. - c.-4088_-4087del r.(?) p.(=)
SLC12A4 NM_005072.4 -/. - c.*4003_*4004del r.(=) p.(=)


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