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Variant : CV734004 (NM_001330700.1(TOP2B):c.3153C>T (p.Tyr1051=)) Homo sapiens

Symbol: CV734004
Name: NM_001330700.1(TOP2B):c.3153C>T (p.Tyr1051=)
Condition: not provided [RCV000907798]
Clinical Significance: likely benign
Last Evaluated: 07/27/2018
Review Status: criteria provided, single submitter
Related Genes: TOP2B  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_001068.3:c.3138C>T
NM_001330700.1:c.3153C>T
NG_052961.1:g.50613C>T
NC_000003.12:g.25618760G>A
NC_000003.11:g.25660251G>A
NP_001059.2:p.Tyr1046=
NP_001317629.1:p.Tyr1051=
Position
Human AssemblyChrPosition (strand)Source
GRCh38325,618,760 - 25,618,760CLINVAR
GRCh37325,660,251 - 25,660,251CLINVAR
Cytogenetic Map33p24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 15182340
Created: 2020-01-07
Species: Homo sapiens
Last Modified: 2020-05-19
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.