All variants in the GDNF gene

Information The variants shown are described using the NM_000514.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.*1389A>G r.(=) p.(=) - likely benign g.37814364T>C g.37814262T>C - - GDNF_000003 65 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs78613670 Germline - 65/2795 individuals - 0 - Mohammed Faruq
-?/. - c.*1389A>G r.(=) p.(=) - likely benign g.37814364T>C g.37814262T>C - - GDNF_000003 3 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs78613670 Germline - 3/2795 individuals - 0 - Mohammed Faruq
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