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Variant : CV434622 (NM_033017.4(TRIM4):c.1450del (p.Trp484fs)) Homo sapiens

Symbol: CV434622
Name: NM_033017.4(TRIM4):c.1450del (p.Trp484fs)
Condition: not provided [RCV000509411]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: TRIM4  
Variant Type: deletion (SO:0001589)
Source: CLINVAR
Molecular Consequence: frameshift variant
Evidence: phenotyping only
HGVS Name(s): NM_033091.3:c.1372del
NM_033017.4:c.1450del
NC_000007.14:g.99892222del
NC_000007.13:g.99489845del
NM_033017.3:c.1450delT
NP_149082.1:p.Trp458fs
NP_148977.2:p.Trp484fs
Position
Human AssemblyChrPosition (strand)Source
GRCh38799,892,216 - 99,892,216CLINVAR
GRCh37799,489,839 - 99,489,839CLINVAR
Cytogenetic Map77q22.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13442781
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.