Variant #0000877957 (NC_000009.11:g.6554673C>T, NM_000170.2:c.2311G>A (GLDC))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6554673C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID GLDC_000061 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs386833553
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-09-10 08:01:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Enzyme activity     
GLDC NM_000170.2 +?/. - c.2311G>A r.(?) p.(Gly771Arg) -


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