Variant #0000299605 (NC_000019.9:g.11123738C>T, NM_003072.3:c.2388C>T (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.11123738C>T
DNA change (hg38) g.11013062C>T
Published as SMARCA4(NM_001128844.1):c.2388C>T (p.(Leu796=)), SMARCA4(NM_001128844.3):c.2388C>T (p.L796=)
ISCN -
DB-ID SMARCA4_000031 See all 7 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) 0.01072 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA4 NM_003072.3 -/. - c.2388C>T r.(?) p.(Leu796=)


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