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Variant : CV662130 (NM_032861.4(SERAC1):c.355+211C>T) Homo sapiens

Symbol: CV662130
Name: NM_032861.4(SERAC1):c.355+211C>T
Condition: not provided [RCV000840581]
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.355+211C>T
NG_032889.1:g.24627C>T
NC_000006.12:g.158148654G>A
NC_000006.11:g.158569686G>A
NM_032861.3:c.355+211C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh386158,148,654 - 158,148,654CLINVAR
GRCh376158,569,686 - 158,569,686CLINVAR
Cytogenetic Map66q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14740991
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.