Variant #0001051066 (NC_000002.11:g.217329363C>T, NM_001127207.1:c.2114C>T (SMARCAL1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.217329363C>T
DNA change (hg38) -
Published as SMARCAL1(NM_014140.3):c.2114C>T (p.T705I), SMARCAL1(NM_014140.4):c.2114C>T (p.(Thr705Ile))
ISCN -
DB-ID SMARCAL1_000018 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.2114C>T r.(?) p.(Thr705Ile)
SMARCAL1 NM_014140.3 +?/. - c.2114C>T r.(?) p.(Thr705Ile)


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