Variant #0000727762 (NC_000020.10:g.57415491_57415514dup, NM_000516.4:c.-51291_-51268dup (GNAS))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57415491_57415514dup
DNA change (hg38) -
Published as GNAS(NM_016592.5):c.330_353dupGACCGAGAGCGAGACCGAGTCCGA (p.T111_E118dup)
ISCN -
DB-ID GNAS-AS1_000006
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAS NM_000516.4 ?/. - c.-51291_-51268dup r.(?) p.(=)
GNAS NM_016592.2 ?/. - c.330_353dup r.(?) p.(Thr111_Glu118dup)
GNAS NM_080425.2 ?/. - c.-12830_-12807dup r.(?) p.(=)
GNAS-AS1 NR_002785.2 ?/. - n.819+1481_819+1504dup r.(?) -


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