Variant #0000720067 (NC_000005.9:g.111071125A>C, NM_139164.1:c.-223052T>G (STARD4))

Chromosome 5
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.111071125A>C
DNA change (hg38) -
Published as NREP(NM_001142483.1):c.81+2T>G
ISCN -
DB-ID STARD4_000001
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NREP NM_004772.2 ?/. - c.81+2T>G r.spl? p.?
STARD4 NM_139164.1 ?/. - c.-223052T>G r.(?) p.(=)
STARD4-AS1 NR_040093.1 ?/. - n.4102+582A>C r.(?) -


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