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Variant : CV368488 (NM_032861.4(SERAC1):c.1308+7G>A) Homo sapiens

Symbol: CV368488
Name: NM_032861.4(SERAC1):c.1308+7G>A
Condition: not specified [RCV000439010]
Clinical Significance: likely benign
Last Evaluated: 09/08/2016
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.54259G>A
NC_000006.12:g.158119022C>T
NC_000006.11:g.158540054C>T
NM_032861.4:c.1308+7G>A
NM_032861.3:c.1308+7G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh386158,119,022 - 158,119,022CLINVAR
GRCh376158,540,054 - 158,540,054CLINVAR
Cytogenetic Map66q25.3CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12844996
Created: 2017-04-11
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.