Variant #0000804356 (NC_000010.10:g.135213094A>G, NM_138384.2:c.482A>G (MTG1))

Chromosome 10
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.135213094A>G
DNA change (hg38) -
Published as MTG1(NM_138384.4):c.482A>G (p.N161S)
ISCN -
DB-ID MTG1_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPRN NM_001012508.3 ?/. - c.*23636T>C r.(=) p.(=)
MTG1 NM_138384.2 ?/. - c.482A>G r.(?) p.(Asn161Ser)


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