Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV108822 (NM_006092.4(NOD1):c.-211+198G>A) Homo sapiens

Symbol: CV108822
Name: NM_006092.4(NOD1):c.-211+198G>A
Condition: not provided [RCV000089347]
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.24075G>A
NC_000007.14:g.30459703C>T
NC_000007.13:g.30499319C>T
NM_001354849.1:c.-211+198G>A
NM_006092.4:c.-211+198G>A
NM_006092.2:c.-211+198G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38730,459,703 - 30,459,703CLINVAR
GRCh37730,499,319 - 30,499,319CLINVAR
Cytogenetic Map77p14.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8648661
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.