Variant #0000256024 (NC_000012.11:g.100656131A>G, NM_017988.4:c.-5468A>G (SCYL2))

Chromosome 12
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.100656131A>G
DNA change (hg38) g.100262353A>G
Published as DEPDC4(NM_152317.3):c.611T>C (p.I204T)
ISCN -
DB-ID DEPDC4_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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCYL2 NM_017988.4 ?/. - c.-5468A>G r.(?) p.(=)
ACTR6 NM_022496.4 ?/. - c.*38438A>G r.(=) p.(=)
DEPDC4 NM_152317.2 ?/. - c.611T>C r.(?) p.(Ile204Thr)


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