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Variant : CV267665 (NM_003179.2(SYP):c.*1T>A) Homo sapiens

Symbol: CV267665
Name: NM_003179.2(SYP):c.*1T>A
Condition: not specified [RCV000285476]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2015
Review Status: criteria provided, single submitter
Related Genes: SYP  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NM_003179.2:c.*1T>A
NG_012532.1:g.13769T>A
NC_000023.11:g.49191436A>T
NC_000023.10:g.49047893A>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38X49,191,436 - 49,191,436CLINVAR
GRCh37X49,047,893 - 49,047,893CLINVAR
Cytogenetic MapXXp11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11637402
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.