Variant #0000607477 (NC_000002.11:g.217293422G>A, NM_001127207.1:c.1251G>A (SMARCAL1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.217293422G>A
DNA change (hg38) g.216428699G>A
Published as SMARCAL1(NM_014140.3):c.1251G>A (p.T417=)
ISCN -
DB-ID SMARCAL1_000049
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCAL1 NM_001127207.1 -?/. - c.1251G>A r.(?) p.(Thr417=)
SMARCAL1 NM_014140.3 -?/. - c.1251G>A r.(?) p.(Thr417=)


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