Variant #0000809389 (NC_000021.8:g.38120214C>A, NM_000411.6:c.*6333G>T (HLCS))

Chromosome 21
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.38120214C>A
DNA change (hg38) -
Published as SIM2(NM_005069.5):c.1825C>A (p.R609S)
ISCN -
DB-ID HLCS_000037
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HLCS NM_000411.6 ?/. - c.*6333G>T r.(=) p.(=)
SIM2 NM_009586.2 ?/. - c.*2640C>A r.(=) p.(=)


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