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Variant : CV506386 (NM_005603.6(ATP8B1):c.771T>C (p.Ala257=)) Homo sapiens

Symbol: CV506386
Name: NM_005603.6(ATP8B1):c.771T>C (p.Ala257=)
Condition: not specified [RCV000602195]
Clinical Significance: likely benign
Last Evaluated: 07/25/2017
Review Status: criteria provided, single submitter
Related Genes: ATP8B1  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NC_000018.10:g.57695460A>G
NC_000018.9:g.55362692A>G
NM_005603.4:c.771T>C
NM_005603.6:c.771T>C
NG_007148.3:g.113363T>C
NP_005594.2:p.Ala257=
LRG_1205t1:c.771T>C
LRG_1205:g.113363T>C
LRG_1205p1:p.Ala257=
NG_007148.2:g.112636T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381857,695,460 - 57,695,460CLINVAR
GRCh371855,362,692 - 55,362,692CLINVAR
Cytogenetic Map1818q21.31CLINVAR
Trait Synonyms: AllHighlyPenetrant




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13535237
Created: 2018-05-08
Species: Homo sapiens
Last Modified: 2019-11-05
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.