Variant #0000566294 (NC_000019.9:g.1399566C>T, NM_000156.5:c.348G>A (GAMT))

Chromosome 19
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.1399566C>T
DNA change (hg38) g.1399567C>T
Published as GAMT(NM_138924.3):c.348G>A (p.L116=)
ISCN -
DB-ID NDUFS7_000021
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) 0.00394 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 09:48:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAMT NM_000156.5 -/. - c.348G>A r.(?) p.(Leu116=)
NDUFS7 NM_024407.4 -/. - c.*4079C>T r.(=) p.(=)


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