Variant #0000888149 (NC_000008.10:g.12957647G>A, NM_182643.2:c.2199C>T (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.12957647G>A
DNA change (hg38) -
Published as DLC1(NM_182643.3):c.2199C>T (p.S733=)
ISCN -
DB-ID DLC1_000026
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) 0.00246 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8orf48 NM_001007090.2 -?/. - c.-466854G>A r.(?) p.(=)
DLC1 NM_182643.2 -?/. - c.2199C>T r.(?) p.(Ser733=)


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