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Variant : CV194911 (NM_003179.2(SYP):c.612G>A (p.Ser204=)) Homo sapiens

Symbol: CV194911
Name: NM_003179.2(SYP):c.612G>A (p.Ser204=)
Condition: not specified [RCV000178874]
Clinical Significance: uncertain significance
Last Evaluated: 12/03/2014
Review Status: criteria provided, single submitter
Related Genes: SYP  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NC_000023.10:g.49049732C>T
NM_003179.2:c.612G>A
NG_012532.1:g.11930G>A
NC_000023.11:g.49193275C>T
NP_003170.1:p.Ser204=
Position
Human AssemblyChrPosition (strand)Source
GRCh38X49,193,275 - 49,193,275CLINVAR
GRCh37X49,049,732 - 49,049,732CLINVAR
Cytogenetic MapXXp11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 10052501
Created: 2015-07-14
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.