Annotation Detail
Information
- Associated Genes
- APC
- Associated Variants
-
APC p.Gln1096Ter (p.Q1096*)
(
ENST00000257430.9,
ENST00000504915.3,
ENST00000507379.6,
ENST00000508376.6,
ENST00000509732.6,
ENST00000512211.7,
ENST00000713638.1,
ENST00000713639.1 )
APC p.Gln1096Ter (p.Q1096*) ( ENST00000257430.9, ENST00000504915.3, ENST00000507379.6, ENST00000508376.6, ENST00000509732.6, ENST00000512211.7, ENST00000713638.1, ENST00000713639.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000038.6(APC):c.3286C>T (p.Gln1096Ter) AND not provided
- ClinVar Allele ID
- 166240
- ClinVar RefSeq Alternation Syntax
- NM_001354898.2:c.3211C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354901.2:c.3109C>T
- ClinVar RefSeq Alternation Syntax
- NM_000038.6:c.3286C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127511.3:c.3232C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354895.2:c.3286C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354905.2:c.2806C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354899.2:c.3202C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354897.2:c.3316C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354906.2:c.2437C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354900.2:c.3163C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354903.2:c.2983C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354902.2:c.3013C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354904.2:c.2908C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354896.2:c.3340C>T
- ClinVar RefSeq Alternation Syntax
- NM_001127510.3:c.3286C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000202095
- ClinVar Disease
- not provided
- Observed Origin Sample
- unknown
Drugs