Variant #0000923962 (NC_000003.11:g.47702889T>C, NM_003074.3:c.2215A>G (SMARCC1))

Chromosome 3
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.47702889T>C
DNA change (hg38) -
Published as SMARCC1(NM_003074.4):c.2215A>G (p.K739E)
ISCN -
DB-ID SMARCC1_000016
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCC1 NM_003074.3 ?/. - c.2215A>G r.(?) p.(Lys739Glu)
SMARCC1 NM_003074.4 ?/. - c.2215A>G r.(?) p.(Lys739Glu)


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