Variant #0001002378 (NC_000016.9:g.48395696C>A, NM_001006610.1:c.737G>T (SIAH1))

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.48395696C>A
DNA change (hg38) -
Published as SIAH1(NM_001006610.2):c.737G>T (p.R246L)
ISCN -
DB-ID LONP2_000002
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
SIAH1 NM_001006610.1 ?/. - c.737G>T r.(?) p.(Arg246Leu)
LONP2 NM_031490.2 ?/. - c.*9983C>A r.(=) p.(=)


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