Annotation

Position
chr11 : 111959726
Genotype
T/A
Gene

HGVS DNA code
HGVS=SDHD:NM_003002:exon3:c.305A>T:p.H102L,
HGVS protein code
OMIM-ID
Pubmed Links
MutationTaster

Author:
GeneTalk
dbSNP Flags:
- Has 3D structure (SNP3D table)
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Weight=1. (Weight on NCBI reference assembly.)
- RS Cluster has none TGP Submission(set VCF OTHERKG).
- Submitted from a locus-specific database.
- Has OMIM/OMIA
- Single base polymorphism SNP

Created at March 09, 2013 16:28, Last update March 09, 2013 16:28
Voting
Pathogenic
Clinical significance
Pathogenic
Votes
StarsClinical significance
53 votes
40 votes
30 votes
20 votes
10 votes

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