Variant #0001056468 (NC_000019.9:g.11098463A>C, NM_003072.3:c.981A>C (SMARCA4))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11098463A>C
DNA change (hg38) -
Published as SMARCA4(NM_001128844.1):c.981A>C (p.P327=), SMARCA4(NM_001128844.3):c.981A>C (p.P327=), SMARCA4(NM_003072.5):c.981A>C (p.(Pro327=))
ISCN -
DB-ID SMARCA4_000109 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) 0.00302 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     
SMARCA4 NM_003072.3 -/. - c.981A>C r.(?) p.(Pro327=)


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