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Variant : CV379956 (NM_001204527.2(SSR4):c.11-21G>A) Homo sapiens

Symbol: CV379956
Name: NM_001204527.2(SSR4):c.11-21G>A
Condition: not specified [RCV000433721]
Clinical Significance: likely benign
Last Evaluated: 07/21/2016
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.20-21G>A
NG_041795.1:g.5479G>A
NC_000023.11:g.153794653G>A
NC_000023.10:g.153060108G>A
NM_001204527.2:c.11-21G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38X153,794,653 - 153,794,653CLINVAR
GRCh37X153,060,108 - 153,060,108CLINVAR
Cytogenetic MapXXq28CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12842058
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.