Variant #0000849710 (NC_000002.11:g.217297448A>G, NM_001127207.1:c.1342A>G (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.217297448A>G
DNA change (hg38) -
Published as SMARCAL1(NM_014140.3):c.1342A>G (p.I448V)
ISCN -
DB-ID SMARCAL1_000062
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCAL1 NM_001127207.1 ?/. - c.1342A>G r.(?) p.(Ile448Val)
SMARCAL1 NM_014140.3 ?/. - c.1342A>G r.(?) p.(Ile448Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.