Variant #0001039361 (NC_000012.11:g.56559114G>C, NM_003075.3:c.3127C>G (SMARCC2))

Chromosome 12
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.56559114G>C
DNA change (hg38) -
Published as SMARCC2(NM_001330288.2):c.3220C>G (p.(Pro1074Ala))
ISCN -
DB-ID MYL6_000010
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) 0.00177 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 2025-05-05 21:14:00 +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     
SMARCC2 NM_003075.3 -?/. - c.3127C>G r.(?) p.(Pro1043Ala)
MYL6 NM_021019.4 -?/. - c.*3960G>C r.(=) p.(=)


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