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Variant : CV669836 (NM_004208.4(AIFM1):c.605+262T>G) Homo sapiens

Symbol: CV669836
Name: NM_004208.4(AIFM1):c.605+262T>G
Condition: not provided [RCV000832345]
Clinical Significance: likely benign
Last Evaluated: 06/14/2018
Review Status: criteria provided, single submitter
Related Genes: AIFM1   RAB33A  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_145812.2:c.593+262T>G
NM_001130847.3:c.605+262T>G
NM_004208.4:c.605+262T>G
NG_013217.1:g.23603T>G
NC_000023.11:g.130147231A>C
NC_000023.10:g.129281206A>C
NM_004208.3:c.605+262T>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38X130,147,231 - 130,147,231CLINVAR
GRCh37X129,281,206 - 129,281,206CLINVAR
Cytogenetic MapXXq26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14723004
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-11-05
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.