Variant #0000253258 (NC_000020.10:g.2375262A>G, NM_198994.2:c.172A>G (TGM6))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2375262A>G
DNA change (hg38) g.2394616A>G
Published as TGM6(NM_198994.2):c.172A>G (p.M58V), TGM6(NM_198994.3):c.172A>G (p.M58V)
ISCN -
DB-ID TGM6_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) 0.90617 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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     
TGM6 NM_198994.2 -/. - c.172A>G r.(?) p.(Met58Val)


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