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Variant : CV661635 (NM_032861.4(SERAC1):c.356-216C>T) Homo sapiens

Symbol: CV661635
Name: NM_032861.4(SERAC1):c.356-216C>T
Condition: not provided [RCV000830908]
Clinical Significance: benign
Last Evaluated: 06/14/2018
Review Status: criteria provided, single submitter
Related Genes: SERAC1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NG_032889.1:g.26152C>T
NC_000006.12:g.158147129G>A
NC_000006.11:g.158568161G>A
NM_032861.3:c.356-216C>T
NM_032861.4:c.356-216C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh386158,147,129 - 158,147,129CLINVAR
GRCh376158,568,161 - 158,568,161CLINVAR
Cytogenetic Map66q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14719723
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-12-03
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.