Variant #0000998329 (NC_000010.10:g.5788197C>T, NM_001494.3:c.*19772G>A (GDI2))

Chromosome 10
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.5788197C>T
DNA change (hg38) -
Published as FAM208B(NM_017782.4):c.2813C>T (p.(Ser938Leu))
ISCN -
DB-ID GDI2_000013
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) 0.00029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDI2 NM_001494.3 -?/. - c.*19772G>A r.(=) p.(=)
FAM208B NM_017782.4 -?/. - c.2813C>T r.(?) p.(Ser938Leu)


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