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Variant : CV108842 (NM_006092.4(NOD1):c.254T>A (p.Phe85Tyr)) Homo sapiens

Symbol: CV108842
Name: NM_006092.4(NOD1):c.254T>A (p.Phe85Tyr)
Condition: not provided [RCV000089367]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: NOD1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense|missense variant
Evidence: literature only|not provided
HGVS Name(s): NG_013025.1:g.28519T>A
NC_000007.14:g.30455259A>T
NC_000007.13:g.30494875A>T
NP_006083.1:p.Phe85Tyr
NM_001354849.1:c.254T>A
NM_006092.4:c.254T>A
NR_149002.1:n.866T>A
NM_006092.2:c.254T>A
NP_001341778.1:p.Phe85Tyr
Position
Human AssemblyChrPosition (strand)Source
GRCh38730,455,259 - 30,455,259CLINVAR
GRCh37730,494,875 - 30,494,875CLINVAR
Cytogenetic Map77p14.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8648681
Created: 2014-05-13
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.