Variant #0000298385 (NC_000009.11:g.2039815_2039817del, NM_003070.3:c.705_707del (SMARCA2))

Chromosome 9
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.2039815_2039817del
DNA change (hg38) g.2039815_2039817del
Published as SMARCA2(NM_003070.3):c.667_669del (p.(Gln225del)), SMARCA2(NM_003070.4):c.705_707delGCA (p.Q238del), SMARCA2(NM_003070.5):c.705_707delGCA (p.Q238del)
ISCN -
DB-ID SMARCA2_000065 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA2 NM_003070.3 -/. - c.705_707del r.(?) p.(Gln238del)


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