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Variant : CV698877 (NM_002588.4(PCDHGC3):c.2431-3554T>C) Homo sapiens

Symbol: CV698877
Name: NM_002588.4(PCDHGC3):c.2431-3554T>C
Condition: not provided [RCV000956316]
Clinical Significance: benign
Last Evaluated: 11/16/2017
Review Status: criteria provided, single submitter
Related Genes: PCDHG@   PCDHGA1   PCDHGA10   PCDHGA11   PCDHGA12   PCDHGA2   PCDHGA3   PCDHGA4   PCDHGA5   PCDHGA6   PCDHGA7   PCDHGA8   PCDHGA9   PCDHGB1   PCDHGB2   PCDHGB3   PCDHGB4   PCDHGB5   PCDHGB6   PCDHGB7   PCDHGC3   PCDHGC4   PCDHGC5  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_032092.2:c.1879-3554T>C
NM_018929.3:c.2013T>C
NM_032407.1:c.2013T>C
NM_003736.3:c.2398-3554T>C
NM_018925.2:c.2398-3554T>C
NM_018922.2:c.2410-3554T>C
NM_018924.5:c.2416-3554T>C
NM_018927.4:c.2416-3554T>C
NM_018926.2:c.2419-3554T>C
NM_018912.2:c.2422-3554T>C
NM_018918.2:c.2422-3554T>C
NM_018923.2:c.2422-3554T>C
NM_003735.3:c.2425-3554T>C
NM_018915.4:c.2425-3554T>C
NM_018916.4:c.2425-3554T>C
NM_018919.3:c.2425-3554T>C
NM_018920.4:c.2425-3554T>C
NM_018921.2:c.2425-3554T>C
NM_032088.1:c.2425-3554T>C
NM_002588.4:c.2431-3554T>C
NM_018914.3:c.2434-3554T>C
NM_018913.2:c.2437-3554T>C
NM_018928.2:c.2443-3554T>C
NM_018917.4:c.2515-3554T>C
NM_032403.3:c.31-3554T>C
NG_050746.1:g.11080T>C
NG_000012.2:g.201450T>C
NC_000005.10:g.141491253T>C
NC_000005.9:g.140870820T>C
NM_018929.2:c.2013T>C
NP_061752.1:p.Pro671=
NP_115783.1:p.Pro671=
Position
Human AssemblyChrPosition (strand)Source
GRCh385141,491,253 - 141,491,253CLINVAR
GRCh375140,870,820 - 140,870,820CLINVAR
Cytogenetic Map55q31.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 15196908
Created: 2020-01-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.