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Variant : CV372690 (NM_001258392.3(CLPB):c.921C>T (p.Phe307=)) Homo sapiens

Symbol: CV372690
Name: NM_001258392.3(CLPB):c.921C>T (p.Phe307=)
Condition: not specified [RCV000418403]
Clinical Significance: likely benign
Last Evaluated: 11/10/2016
Review Status: criteria provided, single submitter
Related Genes: CLPB  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NG_042130.1:g.122512C>T
NC_000011.10:g.72317173G>A
NC_000011.9:g.72028217G>A
NP_110440.1:p.Phe337=
NP_001245321.1:p.Phe307=
LRG_1338t1:c.921C>T
NM_030813.6:c.1011C>T
NM_001258393.3:c.834C>T
NM_001258394.2:c.876C>T
NM_001258392.3:c.921C>T
LRG_1338:g.122512C>T
NG_042130.2:g.122512C>T
NM_030813.5:c.1011C>T
LRG_1338p1:p.Phe307=
NP_001245322.1:p.Phe278=
NP_001245323.1:p.Phe292=
Position
Human AssemblyChrPosition (strand)Source
GRCh381172,317,173 - 72,317,173CLINVAR
GRCh371172,028,217 - 72,028,217CLINVAR
Cytogenetic Map1111q13.4CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12833391
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.