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Variant : CV92901 (NR_027033.2(MIRLET7BHG):n.432T>C) Homo sapiens

Symbol: CV92901
Name: NR_027033.2(MIRLET7BHG):n.432T>C
Condition: Malignant melanoma [RCV000072999]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: MIR4763   MIRLET7A3   MIRLET7B   MIRLET7BHG  
Variant Type: single nucleotide variant (SO:0001619)
Source: CLINVAR
Molecular Consequence: non-coding transcript variant
Evidence: literature only|not provided
HGVS Name(s): NC_000022.11:g.46109326T>C
NC_000022.10:g.46505206T>C
NR_039920.1:c.1-u4240T>C
NR_029478.1:c.1-u3423T>C
NR_027033.1:c.432T>C
NR_029479.1:c.1-u4360T>C
XR_041674.1:c.209T>C
NR_027033.2:n.432T>C
NR_027033.1:n.432T>C
NC_000022.9:g.44883870T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh382246,109,326 - 46,109,326CLINVAR
GRCh372246,505,206 - 46,505,206CLINVAR
Build 362244,883,870 - 44,883,870CLINVAR
Cytogenetic Map2222q13.31CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8637675
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
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.