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Variant : CV352351 (NM_000268.3(NF2):c.*768_*769dup) Homo sapiens

Symbol: CV352351
Name: NM_000268.3(NF2):c.*768_*769dup
Condition: Neurofibromatosis, type 2 [RCV000331790]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: NF2  
Variant Type: duplication (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): NM_181830.3:c.*828_*829dup
NM_181833.2:c.*768_*769dup
NM_181828.3:c.*828_*829dup
NM_016418.5:c.*828_*829dup
NG_009057.1:g.97015_97016dup
LRG_511t2:c.*828_*829dup
LRG_511:g.97015_97016dup
LRG_511t1:c.*768_*769dup
NM_000268.3:c.*768_*769dup
NM_181829.3:c.*828_*829dup
NC_000022.11:g.29695570_29695571dup
NC_000022.10:g.30091559_30091560dup
NR_156186.1:n.3115_3116dup
NM_181832.3:c.*843_*844dup
NM_000268.3:c.*768_*769dupAG
Position
Human AssemblyChrPosition (strand)Source
GRCh382229,695,570 - 29,695,571CLINVAR
GRCh372230,091,559 - 30,091,560CLINVAR
Cytogenetic Map2222q12.2CLINVAR
Age Of Onset: all ages
Prevalence: 1-9 / 100 000



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11656207
Created: 2017-01-11
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.