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Variant : CV704255 (NM_004758.4(TSPOAP1):c.3911G>A (p.Cys1304Tyr)) Homo sapiens

Symbol: CV704255
Name: NM_004758.4(TSPOAP1):c.3911G>A (p.Cys1304Tyr)
Condition: not provided [RCV000954513]
Clinical Significance: likely benign
Last Evaluated: 07/11/2018
Review Status: criteria provided, single submitter
Related Genes: TSPOAP1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_024418.3:c.3731G>A
NM_001261835.2:c.3911G>A
NM_004758.4:c.3911G>A
NC_000017.11:g.58309361C>T
NC_000017.10:g.56386722C>T
NM_004758.3:c.3911G>A
NP_077729.1:p.Cys1244Tyr
NP_001248764.1:p.Cys1304Tyr
NP_004749.2:p.Cys1304Tyr
Position
Human AssemblyChrPosition (strand)Source
GRCh381758,309,361 - 58,309,361CLINVAR
GRCh371756,386,722 - 56,386,722CLINVAR
Cytogenetic Map1717q22CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 15190562
Created: 2020-01-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.