Variant #0000690414 (NC_000009.11:g.131037693G>C, NC_000009.11(NM_004486.4):c.84+479C>G (GOLGA2))

Chromosome 9
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.131037693G>C
DNA change (hg38) -
Published as SWI5(NM_001318092.1):c.7G>C (p.E3Q)
ISCN -
DB-ID GOLGA2_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SWI5 NM_001040011.1 ?/. - c.-732G>C r.(?) p.(=)
GOLGA2 NM_004486.4 ?/. - c.84+479C>G r.(=) p.(=)


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