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Variant : CV377880 (NM_006280.3(SSR4):c.417+15C>T) Homo sapiens

Symbol: CV377880
Name: NM_006280.3(SSR4):c.417+15C>T
Condition: not specified [RCV000429963]
Clinical Significance: uncertain significance
Last Evaluated: 01/10/2017
Review Status: criteria provided, single submitter
Related Genes: SSR4  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_001204526.1:c.450+15C>T
NG_041795.1:g.8977C>T
NC_000023.11:g.153798151C>T
NC_000023.10:g.153063606C>T
NM_006280.3:c.417+15C>T
NM_001204527.2:c.441+15C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38X153,798,151 - 153,798,151CLINVAR
GRCh37X153,063,606 - 153,063,606CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12840052
Created: 2017-04-11
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.