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Variant : CV108831 (NM_006092.4(NOD1):c.2285+112G>A) Homo sapiens

Symbol: CV108831
Name: NM_006092.4(NOD1):c.2285+112G>A
Condition: not provided [RCV000089356]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: NOD1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NG_013025.1:g.35592G>A
NC_000007.14:g.30448186C>T
NC_000007.13:g.30487802C>T
NM_001354849.1:c.2285+112G>A
NM_006092.4:c.2285+112G>A
NM_006092.2:c.2285+112G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38730,448,186 - 30,448,186CLINVAR
GRCh37730,487,802 - 30,487,802CLINVAR
Cytogenetic Map77p14.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8648670
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.