Variant #0000525690 (NC_000005.9:g.37815756G>C, NM_000514.3:c.633C>G (GDNF))

Chromosome 5
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.37815756G>C
DNA change (hg38) g.37815654G>C
Published as GDNF(NM_000514.3):c.633C>G (p.(Ile211Met)), GDNF(NM_001190468.1):c.684C>G (p.I228M)
ISCN -
DB-ID GDNF_000002 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) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GDNF NM_000514.3 ?/. - c.633C>G r.(?) p.(Ile211Met)


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