Variant #0000514529 (NC_000002.11:g.217281004T>C, NM_001127207.1:c.836T>C (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.217281004T>C
DNA change (hg38) g.216416281T>C
Published as SMARCAL1(NM_014140.3):c.836T>C (p.F279S)
ISCN -
DB-ID SMARCAL1_000004 See all 2 reported entries
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) 0.00011 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCAL1 NM_001127207.1 ?/. - c.836T>C r.(?) p.(Phe279Ser)
SMARCAL1 NM_014140.3 ?/. - c.836T>C r.(?) p.(Phe279Ser)


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