Variant #0001032048 (NC_000001.10:g.41483673G>T, NM_001031694.2:c.*10193C>A (SCMH1))

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.41483673G>T
DNA change (hg38) -
Published as SLFNL1(NM_144990.4):c.591C>A (p.(Ser197=))
ISCN -
DB-ID SCMH1_000004
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCMH1 NM_001031694.2 ?/. - c.*10193C>A r.(=) p.(=)
SLFNL1 NM_144990.3 ?/. - c.591C>A r.(?) p.(=)
SLFNL1-AS1 NR_037868.1 ?/. - n.3412G>T r.(?) -


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