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Variant : CV339363 (NM_003179.2(SYP):c.877G>A (p.Gly293Ser)) Homo sapiens

Symbol: CV339363
Name: NM_003179.2(SYP):c.877G>A (p.Gly293Ser)
Condition: History of neurodevelopmental disorder [RCV000721022]|Neurodevelopmental [RCV000721022]|Non-syndromic X-linked intellectual disability [RCV000376099]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: SYP  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_003179.2:c.877G>A
NG_012532.1:g.13703G>A
NC_000023.11:g.49191502C>T
NC_000023.10:g.49047959C>T
NP_003170.1:p.Gly293Ser
P08247:p.Gly293Ser
Position
Human AssemblyChrPosition (strand)Source
GRCh38X49,191,502 - 49,191,502CLINVAR
GRCh37X49,047,959 - 49,047,959CLINVAR
Cytogenetic MapXXp11.23CLINVAR
Trait Synonyms: Mental retardation, nonsyndromic, X-linked; X-linked mental retardation; X-linked non-specific intellectual disability



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11623706
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.