Annotation Detail
Information
- Associated Genes
- FGFR2
- Associated Variants
-
FGFR2 p.Pro263Leu (p.P263L)
(
ENST00000369060.8,
ENST00000369061.8,
ENST00000369056.5,
ENST00000360144.7,
ENST00000369059.5,
ENST00000346997.6,
ENST00000351936.11,
ENST00000457416.7,
ENST00000478859.5,
ENST00000358487.10,
ENST00000357555.9,
ENST00000356226.8,
ENST00000613048.4,
ENST00000638709.2,
ENST00000682550.1,
ENST00000682772.1,
ENST00000683211.1,
ENST00000684153.1 )
FGFR2 p.Pro263Leu (p.P263L) ( ENST00000346997.6, ENST00000351936.11, ENST00000356226.8, ENST00000357555.9, ENST00000358487.10, ENST00000360144.7, ENST00000369056.5, ENST00000369059.5, ENST00000369060.8, ENST00000369061.8, ENST00000457416.7, ENST00000478859.5, ENST00000613048.4, ENST00000638709.2, ENST00000682550.1, ENST00000682772.1, ENST00000683211.1, ENST00000684153.1 ) - Associated Disease
- Familial scaphocephaly syndrome, McGillivray type Saethre-Chotzen syndrome Gastric cancer Levy-Hollister syndrome Crouzon syndrome Acrocephalosyndactyly type I Jackson-Weiss syndrome Bent bone dysplasia syndrome 1 Pfeiffer syndrome Beare-Stevenson cutis gyrata syndrome Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
- Source Database
- ClinVar
- Description
- NM_000141.5(FGFR2):c.788C>T (p.Pro263Leu) AND multiple conditions
- ClinVar Allele ID
- 993743
- ClinVar RefSeq Alternation Syntax
- NM_001144914.1:c.749-4811C>T
- ClinVar RefSeq Alternation Syntax
- NR_073009.2:n.1076C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144916.2:c.443C>T
- ClinVar RefSeq Alternation Syntax
- NM_022969.1:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_022970.4:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_023029.2:c.521C>T
- ClinVar RefSeq Alternation Syntax
- NM_000141.5:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144918.2:c.443C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144913.1:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144917.2:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_001320658.2:c.788C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144919.2:c.521C>T
- ClinVar RefSeq Alternation Syntax
- NM_001320654.2:c.104C>T
- ClinVar RefSeq Alternation Syntax
- NM_001144915.2:c.521C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2022-03-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002499544
- ClinVar Disease
- Pfeiffer syndrome
- ClinVar Disease
- Acrocephalosyndactyly type I
- ClinVar Disease
- Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis
- ClinVar Disease
- Saethre-Chotzen syndrome
- ClinVar Disease
- Jackson-Weiss syndrome
- ClinVar Disease
- Bent bone dysplasia syndrome 1
- ClinVar Disease
- Beare-Stevenson cutis gyrata syndrome
- ClinVar Disease
- Familial scaphocephaly syndrome, McGillivray type
- ClinVar Disease
- Gastric cancer
- ClinVar Disease
- Levy-Hollister syndrome
- ClinVar Disease
- Crouzon syndrome
- Observed Origin Sample
- unknown
Drugs