Annotation
Position
chr1 : 197059477
Genotype
AC/A
Gene
HGVS DNA code
HGVS=ASPM:NM_001206846:exon23:c.4923_4924insG:p.C1641fs,ASPM:NM_018136:exon24:c.9678_9679insG:p.C3226fs,
HGVS protein code
Author:
GeneTalk
dbSNP Flags:
- Has SubmitterLinkOut (From SNP->SubSNP->Batch.link_out)
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Has non-synonymous frameshift (A coding region variation where one allele in the set changes all downstream amino acids. FxnClass = 44)
- Has reference (A coding region variation where one allele in the set is identical to the reference sequence. FxnCode = 8)
- 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
- dips (deletion/insertion)
- Single base polymorphism SNP
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Has non-synonymous frameshift (A coding region variation where one allele in the set changes all downstream amino acids. FxnClass = 44)
- Has reference (A coding region variation where one allele in the set is identical to the reference sequence. FxnCode = 8)
- 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
- dips (deletion/insertion)
- Single base polymorphism SNP
Created at March 09, 2013 13:08, Last update March 09, 2013 13:08
Voting
Clinical significance
Pathogenic
Votes
| Stars | Clinical significance |
|---|---|
| 5 | 3 votes |
| 4 | 0 votes |
| 3 | 0 votes |
| 2 | 0 votes |
| 1 | 0 votes |
Comments
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