Annotation Detail
Information
- Associated Genes
- STIM1
- Associated Variants
-
STIM1 p.Asp78= (p.D78=)
(
ENST00000616714.4,
ENST00000698913.1,
ENST00000698910.1,
ENST00000698916.1,
ENST00000698912.1,
ENST00000698911.1,
ENST00000527651.5,
ENST00000525403.6,
ENST00000698915.1,
ENST00000526596.2,
ENST00000698914.1,
ENST00000300737.8 )
STIM1 p.Asp78= (p.D78=) ( ENST00000300737.8, ENST00000525403.6, ENST00000526596.2, ENST00000527651.5, ENST00000616714.4, ENST00000698910.1, ENST00000698911.1, ENST00000698912.1, ENST00000698913.1, ENST00000698914.1, ENST00000698915.1, ENST00000698916.1 ) - Associated Disease
- STIM1-related disorder
- Source Database
- ClinVar
- Description
- NM_001382567.1(STIM1):c.234T>C (p.Asp78=) AND STIM1-related disorder
- ClinVar Allele ID
- 461308
- ClinVar RefSeq Alternation Syntax
- NM_001382577.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382578.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NR_168436.1:n.841T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382568.1:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382581.1:c.-219-56227T>C
- ClinVar RefSeq Alternation Syntax
- NR_168438.1:n.841T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382576.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382575.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382570.1:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382579.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382574.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382571.1:c.-98-56227T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382573.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NR_168437.1:n.841T>C
- ClinVar RefSeq Alternation Syntax
- NM_001277961.3:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382572.1:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382566.1:c.12T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382580.1:c.-219-56227T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382567.1:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_001382569.1:c.136-56227T>C
- ClinVar RefSeq Alternation Syntax
- NM_001277962.2:c.234T>C
- ClinVar RefSeq Alternation Syntax
- NM_003156.4:c.234T>C
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2019-04-25
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003935432
- ClinVar Disease
- STIM1-related disorder
- Observed Origin Sample
- germline
Drugs