Variant #0000533817 (NC_000008.10:g.13425379T>C, NM_182643.2:c.-53394A>G (DLC1))

Chromosome 8
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.13425379T>C
DNA change (hg38) g.13567870T>C
Published as C8orf48(NM_001007090.3):c.879T>C (p.C293=)
ISCN -
DB-ID DLC1_000007
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 17:36:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8orf48 NM_001007090.2 -?/. - c.879T>C r.(?) p.(Cys293=)
DLC1 NM_182643.2 -?/. - c.-53394A>G r.(?) p.(=)


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