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Variant : CV661650 (NM_032861.4(SERAC1):c.129-85C>G) Homo sapiens

Symbol: CV661650
Name: NM_032861.4(SERAC1):c.129-85C>G
Condition: not provided [RCV000835598]
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): NM_032861.4:c.129-85C>G
NG_032889.1:g.22607C>G
NC_000006.12:g.158150674G>C
NC_000006.11:g.158571706G>C
NM_032861.3:c.129-85C>G
Position
Human AssemblyChrPosition (strand)Source
GRCh386158,150,674 - 158,150,674CLINVAR
GRCh376158,571,706 - 158,571,706CLINVAR
Cytogenetic Map66q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14730268
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-11-12
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.