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Variant : CV659939 (NM_182760.4(SUMF1):c.603-156T>C) Homo sapiens

Symbol: CV659939
Name: NM_182760.4(SUMF1):c.603-156T>C
Condition: not provided [RCV000844318]
Clinical Significance: benign
Last Evaluated: 06/19/2018
Review Status: criteria provided, single submitter
Related Genes: SUMF1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_001164674.1:c.528-156T>C
NM_001164675.1:c.603-156T>C
NM_182760.4:c.603-156T>C
NG_016225.1:g.53995T>C
NG_016225.2:g.53995T>C
NC_000003.12:g.4418288A>G
NC_000003.11:g.4459972A>G
NM_182760.3:c.603-156T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh3834,418,288 - 4,418,288CLINVAR
GRCh3734,459,972 - 4,459,972CLINVAR
Cytogenetic Map33p26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14746320
Created: 2019-09-06
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.