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Variant : CV370267 (NM_032861.4(SERAC1):c.1155A>G (p.Gln385=)) Homo sapiens

Symbol: CV370267
Name: NM_032861.4(SERAC1):c.1155A>G (p.Gln385=)
Condition: not specified [RCV000428555]
Clinical Significance: benign
Last Evaluated: 06/09/2015
Review Status: criteria provided, single submitter
Related Genes: SERAC1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NG_032889.1:g.52845A>G
NC_000006.12:g.158120436T>C
NC_000006.11:g.158541468T>C
NP_116250.3:p.Gln385=
NM_032861.4:c.1155A>G
NM_032861.3:c.1155A>G
NR_073096.1:n.1183A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh386158,120,436 - 158,120,436CLINVAR
GRCh376158,541,468 - 158,541,468CLINVAR
Cytogenetic Map66q25.3CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12839297
Created: 2017-04-11
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.