Variant #0000994282 (NC_000004.11:g.38138822C>G, NM_015173.3:c.3373C>G (TBC1D1))

Chromosome 4
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.38138822C>G
DNA change (hg38) -
Published as TBC1D1(NM_015173.3):c.3373C>G (p.(Leu1125Val))
ISCN -
DB-ID PTTG2_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTTG2 NM_006607.2 ?/. - c.*176191C>G r.(=) p.(=)
TBC1D1 NM_015173.3 ?/. - c.3373C>G r.(?) p.(Leu1125Val)


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