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Variant : CV660109 (NM_182760.4(SUMF1):c.841-75C>T) Homo sapiens

Symbol: CV660109
Name: NM_182760.4(SUMF1):c.841-75C>T
Condition: not provided [RCV000844320]
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.766-75C>T
NM_001164675.1:c.841-75C>T
NM_182760.4:c.841-75C>T
NG_016225.1:g.61230C>T
NG_016225.2:g.61230C>T
NC_000003.12:g.4411053G>A
NC_000003.11:g.4452737G>A
NM_182760.3:c.841-75C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3834,411,053 - 4,411,053CLINVAR
GRCh3734,452,737 - 4,452,737CLINVAR
Cytogenetic Map33p26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14746322
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-12-03
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.