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Variant : CV84422 (NM_000228.2(LAMB3):c.2640G>A (p.Gln880=)) Homo sapiens

Symbol: CV84422
Name: NM_000228.2(LAMB3):c.2640G>A (p.Gln880=)
Condition: Malignant melanoma [RCV000064504]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided|not classified by submitter
Related Genes: LAMB3   MIR4260  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: literature only|not provided
HGVS Name(s): NM_000228.2:c.2640G>A
NM_001017402.1:c.2640G>A
NM_001127641.1:c.2640G>A
NG_007116.1:g.34879G>A
NC_000001.11:g.209622597C>T
NC_000001.10:g.209795942C>T
NR_036213.1:c.67+d847G>A
NP_000219.2:p.Gln880=
NP_001017402.1:p.Gln880=
NP_001121113.1:p.Gln880=
NC_000001.9:g.207862565C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381209,622,597 - 209,622,597CLINVAR
GRCh371209,795,942 - 209,795,942CLINVAR
Build 361207,862,565 - 207,862,565CLINVAR
Cytogenetic Map11q32.2CLINVAR
Trait Synonyms: Malignant melanoma, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8629277
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.