Variant #0000514534 (NC_000002.11:g.217288388G>C, NM_001127207.1:c.1129G>C (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.217288388G>C
DNA change (hg38) g.216423665G>C
Published as SMARCAL1(NM_001127207.1):c.1129G>C (p.(Glu377Gln)), SMARCAL1(NM_014140.3):c.1129G>C (p.E377Q)
ISCN -
DB-ID SMARCAL1_000011 See all 3 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) 0.03172 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.1129G>C r.(?) p.(Glu377Gln)
SMARCAL1 NM_014140.3 -?/. - c.1129G>C r.(?) p.(Glu377Gln)


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