Variant #0000975832 (NC_000003.11:g.44955174T>C, NM_003241.3:c.2012T>C (TGM4))

Chromosome 3
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.44955174T>C
DNA change (hg38) -
Published as TGM4(NM_003241.4):c.2012T>C (p.(Val671Ala))
ISCN -
DB-ID TGM4_000005
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) 0.00022 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGM4 NM_003241.3 ?/. - c.2012T>C r.(?) p.(Val671Ala)
ZDHHC3 NM_016598.2 ?/. - c.*13007A>G r.(=) p.(=)


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