Variant #0001002490 (NC_000016.9:g.67969976_67969977insTA, NM_000229.1:c.*3830_*3831insTA (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.67969976_67969977insTA
DNA change (hg38) -
Published as PSMB10(NM_002801.3):c.272_273insTA (p.(Glu92fs))
ISCN -
DB-ID CTRL_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*3830_*3831insTA r.(=) p.(=)
CTRL NM_001907.2 ?/. - c.-4222_-4221insTA r.(?) p.(=)
PSMB10 NM_002801.3 ?/. - c.272_273insTA r.(?) p.(Glu92Thrfs*3)
SLC12A4 NM_005072.4 ?/. - c.*8766_*8767insTA r.(=) p.(=)
PSKH1 NM_006742.2 ?/. - c.*8431_*8432insTA r.(=) p.(=)


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