Variant #0000800367 (NC_000002.11:g.217311816G>A, NM_001127207.1:c.1786G>A (SMARCAL1))

Chromosome 2
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.217311816G>A
DNA change (hg38) -
Published as SMARCAL1(NM_001127207.1):c.1786G>A (p.(Ala596Thr))
ISCN -
DB-ID SMARCAL1_000056
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) 7.0E-5 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 2021-09-17 14:40:49 +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     
SMARCAL1 NM_001127207.1 ?/. - c.1786G>A r.(?) p.(Ala596Thr)
SMARCAL1 NM_014140.3 ?/. - c.1786G>A r.(?) p.(Ala596Thr)


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