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Variant : CV301038 (NM_007214.4(SEC63):c.-268C>A) Homo sapiens

Symbol: CV301038
Name: NM_007214.4(SEC63):c.-268C>A
Condition: Congenital cystic disease of liver [RCV000277607]|Polycystic liver disease 1 [RCV000277607]|Polycystic liver disease [RCV000277607]
Clinical Significance: likely benign
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: SEC63  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Molecular Consequence: 5 prime utr variant
Evidence: clinical testing
HGVS Name(s): NG_008270.1:g.5002C>A
NC_000006.12:g.107958277G>T
NC_000006.11:g.108279481G>T
NM_007214.4:c.-268C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh386107,958,277 - 107,958,277CLINVAR
GRCh376108,279,481 - 108,279,481CLINVAR
Cytogenetic Map66q21CLINVAR
Trait Synonyms: POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11584962
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.