Variant #0001031504 (NC_000001.10:g.178821952C>G, NM_004673.3:c.1154G>C (ANGPTL1))

Chromosome 1
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.178821952C>G
DNA change (hg38) -
Published as ANGPTL1(NM_004673.4):c.1154G>C (p.(Ser385Thr))
ISCN -
DB-ID ANGPTL1_000005
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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ANGPTL1 NM_004673.3 ?/. - c.1154G>C r.(?) p.(Ser385Thr)
RALGPS2 NM_152663.3 ?/. - c.607+19267C>G r.(=) p.(=)


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