Variant #0000655992 (NC_000008.10:g.12956899_12956919dup, NM_182643.2:c.2927_2947dup (DLC1))

Chromosome 8
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.12956899_12956919dup
DNA change (hg38) g.13099390_13099410dup
Published as DLC1(NM_182643.3):c.2927_2947dupAGCCCTCCGAGATCCCGGAAA (p.E982_R983ins7)
ISCN -
DB-ID DLC1_000010
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-467602_-467582dup r.(?) p.(=)
DLC1 NM_182643.2 ?/. - c.2927_2947dup r.(?) p.(Glu982_Arg983insLysProSerGluIleProGlu)


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