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Variant : CV446542 (NM_001204527.2(SSR4):c.11-94C>G) Homo sapiens

Symbol: CV446542
Name: NM_001204527.2(SSR4):c.11-94C>G
Condition: not specified [RCV000519399]
Clinical Significance: uncertain significance
Last Evaluated: 09/08/2017
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.14C>G
NG_041795.1:g.5406C>G
NC_000023.11:g.153794580C>G
NC_000023.10:g.153060035C>G
NP_001191455.1:p.Pro5Arg
NM_001204527.2:c.11-94C>G
NR_037927.1:n.132C>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38X153,794,580 - 153,794,580CLINVAR
GRCh37X153,060,035 - 153,060,035CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13473494
Created: 2018-01-09
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.