Variant #0000566290 (NC_000019.9:g.1398750C>T, NC_000019.9(NM_000156.5):c.570+165G>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.1398750C>T
DNA change (hg38) g.1398751C>T
Published as GAMT(NM_138924.3):c.735G>A (p.A245=)
ISCN -
DB-ID NDUFS7_000018 See all 2 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) 0.0102 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
GAMT NM_000156.5 -/. - c.570+165G>A r.(=) p.(=)
NDUFS7 NM_024407.4 -/. - c.*3263C>T r.(=) p.(=)


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