Variant #0000679968 (NC_000014.8:g.24731434G>T, NM_000359.2:c.125C>A (TGM1))

Chromosome 14
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.24731434G>T
DNA change (hg38) -
Published as TGM1(NM_000359.3):c.125C>A (p.S42Y)
ISCN -
DB-ID TGM1_000004 See all 3 reported entries
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) 0.00423 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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     
TGM1 NM_000359.2 ?/. - c.125C>A r.(?) p.(Ser42Tyr)
RABGGTA NM_182836.2 ?/. - c.*3387C>A r.(=) p.(=)


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