Variant #0000566296 (NC_000019.9:g.1399955G>A, GAMT(NM_000156.5):c.182-18C>T)

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1399955G>A
DNA change (hg38) g.1399956G>A
Published as GAMT(NM_000156.6):c.182-18C>T
ISCN -
DB-ID NDUFS7_000023
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) 0.00059 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GAMT NM_000156.5 -?/. - c.182-18C>T r.(=) p.(=)
NDUFS7 NM_024407.4 -?/. - c.*4468G>A r.(=) p.(=)