Variant #0000284454 (NC_000017.10:g.42152789C>T, NM_138387.3:c.647C>T (G6PC3))

Chromosome 17
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.42152789C>T
DNA change (hg38) g.44075421C>T
Published as G6PC3(NM_138387.3):c.647C>T (p.(Thr216Ile), p.T216I)
ISCN -
DB-ID G6PC3_000004 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) 0.00312 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC5 NM_001015053.1 -/. - c.*2955G>A r.(=) p.(=)
G6PC3 NM_138387.3 -/. - c.647C>T r.(?) p.(Thr216Ile)


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