Variant #0001042666 (NC_000019.9:g.1399892G>A, NM_000156.5:c.227C>T (GAMT))

Chromosome 19
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.1399892G>A
DNA change (hg38) -
Published as GAMT(NM_000156.6):c.227C>T (p.(Ser76Leu))
ISCN -
DB-ID NDUFS7_000037
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) 0.00026 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 2025-05-05 21:14:00 +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     
GAMT NM_000156.5 ?/. - c.227C>T r.(?) p.(Ser76Leu)
NDUFS7 NM_024407.4 ?/. - c.*4405G>A r.(=) p.(=)


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