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Variant : CV360672 (NM_000390.4(CHM):c.1213C>T (p.Gln405Ter)) Homo sapiens

Symbol: CV360672
Name: NM_000390.4(CHM):c.1213C>T (p.Gln405Ter)
Condition: not provided [RCV000413451]
Clinical Significance: pathogenic
Last Evaluated: 03/03/2016
Review Status: criteria provided, single submitter
Related Genes: CHM  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: nonsense
Evidence: clinical testing
HGVS Name(s): LRG_699:g.141271C>T
NG_009874.2:g.141271C>T
NC_000023.11:g.85911292G>A
NC_000023.10:g.85166297G>A
NP_000381.1:p.Gln405Ter
LRG_699t1:c.1213C>T
NM_000390.4:c.1213C>T
NM_001320959.1:c.769C>T
NM_001362517.1:c.769C>T
NM_001362518.2:c.769C>T
NM_001362519.1:c.769C>T
NM_000390.2:c.1213C>T
NP_001307888.1:p.Gln257Ter
NP_001349446.1:p.Gln257Ter
NP_001349447.1:p.Gln257Ter
NP_001349448.1:p.Gln257Ter
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,911,292 - 85,911,292CLINVAR
GRCh37X85,166,297 - 85,166,297CLINVAR
Cytogenetic MapXXq21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12742343
Created: 2017-02-07
Species: Homo sapiens
Last Modified: 2019-09-10
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.