Variant #0000009037 (NC_000015.10:g.32731153A>G, GREM1(NM_013372.6):c.463A>G)

Individual ID 00001715
Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.32731153A>G
Reference -
DB-ID GREM1_000001
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Pablo Kalfayan-Hospital Italiano
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

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RNA change     

Review status     
GREM1 NM_013372.6 ?/? 3 c.463A>G p.(Thr155Ala) Hetero no =? -



Screenings


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Technique     

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Variants found     

Owner     
0000001993 DNA SEQ-NG Genos Panel (16 genes) APC, AXIN2, BMPR1A, CHEK2, EPCAM, GREM1, MLH1, MSH2, MSH6, MUTYH, NTHL1, PMS2, PTEN, POLE, POLD1, SMAD4, STK11, TP53 28-oct-2020 Multigenetic panel - 2 Pablo Kalfayan-Hospital Italiano