Variant #0000622760 (NC_000012.11:g.100660723A>G, NM_017988.4:c.-876A>G (SCYL2))

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.100660723A>G
DNA change (hg38) g.100266945A>G
Published as DEPDC4(NM_001319311.1):c.132T>C (p.D44=)
ISCN -
DB-ID ACTR6_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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-02 17:50:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCYL2 NM_017988.4 -?/. - c.-876A>G r.(?) p.(=)
ACTR6 NM_022496.4 -?/. - c.*43030A>G r.(=) p.(=)
DEPDC4 NM_152317.2 -?/. - c.132T>C r.(?) p.(Asp44=)


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