USH2A E3411A - GET-Evidence

Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.

To be considered sufficiently evaluated a variant must have both "variant evidence" and "clinical importance" scores filled in.

Please help improve GET-Evidence by evaluating evidence for this variant!

Curation:
Currentness:

USH2A E3411A

(USH2A Glu3411Ala)


Short summary

 

Variant evidence
Computational 2

Variant Effect Predictor (Ensembl ):
SIFT=tolerated(1);
PolyPhen=benign(0);
Condel=not_computable_was(-1)
Mutation Tasting Prediction: Polymorphism p value: 0.999994; (Detail: aa 32-5042 TOPO_DOMAIN Extracellular (potential) gets lost; aa 3404-3494 DOMAIN Fibronectin type-III 19 gets lost)
GVGD: GV 106.71; GD 0.00; Class C0
Multi-alignment of O75445.3 Usher syndrome 2A (autosomal recessive, mild) [Homo sapiens] with: XP_514197.2 [Pan troglodytes] XP_514197.2 [Pan troglodytes] XP_002760562.1 [Callithrix jacchus] XP_001915680.1 [Equus caballus] NP_001178354.1 [Bos taurus] XP_545710.2 [Canis familiaris] XP_002693994.1 [Bos taurus] XP_002924255.1 [Ailuropoda melanoleuca] XP_001375119.1 [Monodelphis domestica] EFB20486.1 [Ailuropoda melanoleuca] NP_067383.3 [Mus musculus]

Functional -
Case/Control -
Familial -
 
Clinical importance
Severity -
Treatability -
Penetrance -
 

Impact

Insufficiently evaluated not reviewed

(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)

Inheritance pattern

unknown

Summary of published research, and additional commentary

 

Allele frequency

  • G @ chr1:215960167: 57.3% (6166/10758) in EVS
  • G @ chr1:214026789: 58.6% (75/128) in GET-Evidence
  • Frequency shown in summary reports: 57.3% (6166/10758)

Publications
 

Genomes
 

hu011C57 - CGI sample GS01669-DNA_B05 from PGP sample 86486261
hom G @ chr1:215960167

 

hu025CEA - CGI sample GS01669-DNA_D02 from PGP sample 27316983
hom G @ chr1:215960167

 

hu04FD18 - CGI sample GS00253-DNA_F01_200_37
het G @ chr1:215960167

 

hu0D879F - CGI sample GS00253-DNA_G01_200_37
hom G @ chr1:215960167

 

 

hu241DEA - CGI sample GS01175-DNA_D05 from PGP sample 1205491
hom G @ chr1:215960167

 

hu2D6140 - CGI sample GS01173-DNA_F06 from PGP sample 64191565
het G @ chr1:215960167

 

 

hu342A08 - CGI sample GS01175-DNA_B05 from PGP sample 83494370
het G @ chr1:215960167

 

 

hu38168C - CGI sample GS01173-DNA_H06 from PGP sample 91708424
hom G @ chr1:215960167

 

hu3CAB43 - CGI sample GS01175-DNA_D03 from PGP sample 27486199
hom G @ chr1:215960167

 

hu4339C0 - CGI sample GS01175-DNA_H01 from PGP sample 94797469
het G @ chr1:215960167

 

hu43860C - CGI sample GS00253-DNA_A01_200_37
hom G @ chr1:215960167

 

hu4CA5B9 - CGI sample GS01669-DNA_B03 from PGP sample 14427241
hom G @ chr1:215960167

 

hu604D39 - CGI sample GS00253-DNA_B02_200_37
hom G @ chr1:215960167

 

 

 

hu8229AE - CGI sample GS01173-DNA_A07 from PGP sample 96240009
het G @ chr1:215960167

 

hu92C40A - CGI sample GS01175-DNA_G03 from PGP sample 92527586
het G @ chr1:215960167

 

hu92FD55 - CGI sample GS01669-DNA_A04 from PGP sample 08188426
hom G @ chr1:215960167

 

hu9385BA - CGI sample GS00253-DNA_E01_200_37
hom G @ chr1:215960167

 

huA0E089 - CGI sample GS01175-DNA_B04 from PGP sample 88590671
het G @ chr1:215960167

 

 

huAE4A11 - CGI sample GS01669-DNA_F02 from PGP sample 40767107
hom G @ chr1:215960167

 

huBAAC98 - CGI sample GS01173-DNA_F02 from PGP sample 70008981
hom G @ chr1:215960167

 

huBEDA0B - CGI sample GS00253-DNA_C01_200_37
het G @ chr1:215960167

 

huC30901 - CGI sample GS00253-DNA_B01_200_37
hom G @ chr1:215960167

 

huCA017E - CGI sample GS01175-DNA_B01 from PGP sample 86206034
het G @ chr1:215960167

 

huD37D14 - CGI sample GS01175-DNA_A04 from PGP sample 13272228
het G @ chr1:215960167

 

huE80E3D - CGI sample GS00253-DNA_D01_200_37
het G @ chr1:215960167

 

huFAF983 - CGI sample GS01175-DNA_F02 from PGP sample 95788191
hom G @ chr1:215960167

 

huFFAD87 - CGI sample GS01669-DNA_H05 from PGP sample 10971581
hom G @ chr1:215960167

 

GS06994 - var-GS06994-1100-36-ASM
het G @ chr1:214026790

 

GS07357 - var-GS07357-1100-36-ASM
het G @ chr1:214026790

 

GS10851 - var-GS10851-1100-36-ASM
het G @ chr1:214026790

 

GS18501 - var-GS18501-1100-36-ASM
het G @ chr1:214026790

 

GS18502 - var-GS18502-1100-36-ASM
het G @ chr1:214026790

 

GS18505 - var-GS18505-1100-36-ASM
het G @ chr1:214026790

 

GS18508 - var-GS18508-1100-36-ASM
het G @ chr1:214026790

 

GS18517 - var-GS18517-1100-36-ASM
het G @ chr1:214026790

 

GS18526 - var-GS18526-1100-36-ASM
het G @ chr1:214026790

 

GS18537 - var-GS18537-1100-36-ASM
hom G @ chr1:214026790

 

GS18555 - var-GS18555-1100-36-ASM
het G @ chr1:214026790

 

GS18558 - var-GS18558-1100-36-ASM
het G @ chr1:214026790

 

GS18940 - var-GS18940-1100-36-ASM
hom G @ chr1:214026790

 

GS18947 - var-GS18947-1100-36-ASM
hom G @ chr1:214026790

 

GS18956 - var-GS18956-1100-36-ASM
het G @ chr1:214026790

 

GS19017 - var-GS19017-1100-36-ASM
hom G @ chr1:214026790

 

GS19020 - var-GS19020-1100-36-ASM
hom G @ chr1:214026790

 

GS19025 - var-GS19025-1100-36-ASM
het G @ chr1:214026790

 

GS19026 - var-GS19026-1100-36-ASM
het G @ chr1:214026790

 

GS19129 - var-GS19129-1100-36-ASM
hom G @ chr1:214026790

 

GS19238 - var-GS19238-1100-36-ASM
hom G @ chr1:214026790

 

GS19239 - var-GS19239-1100-36-ASM
het G @ chr1:214026790

 

GS19240 - var-GS19240-1100-36-ASM
hom G @ chr1:214026790

 

GS19649 - var-GS19649-1100-36-ASM
het G @ chr1:214026790

 

GS19669 - var-GS19669-1100-36-ASM
het G @ chr1:214026790

 

GS19700 - var-GS19700-1100-36-ASM
het G @ chr1:214026790

 

GS19701 - var-GS19701-1100-36-ASM
het G @ chr1:214026790

 

GS19703 - var-GS19703-1100-36-ASM
het G @ chr1:214026790

 

GS19704 - var-GS19704-1100-36-ASM
het G @ chr1:214026790

 

GS19735 - var-GS19735-1100-36-ASM
hom G @ chr1:214026790

 

GS19834 - var-GS19834-1100-36-ASM
het G @ chr1:214026790

 

GS20502 - var-GS20502-1100-36-ASM
het G @ chr1:214026790

 

GS20509 - var-GS20509-1100-36-ASM
hom G @ chr1:214026790

 

GS21767 - var-GS21767-1100-36-ASM
hom G @ chr1:214026790

 

Other external references
 

    dbSNP
  • rs10864198
    www.ncbi.nlm.nih.gov/projects/SNP/snp_ref.cgi
    GeneTests
  • GeneTests records for the USH2A gene
    Retinitis Pigmentosa, Autosomal Recessive
    Usher Syndrome Type 2
    USH2A-Related Retinitis Pigmentosa
    Usher Syndrome Type 2A
    www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/USH2A
    PolyPhen-2
  • Score: 0 (benign)

Other in silico analyses
 

  • NBLOSUM100 score = 3
  • GET-Evidence autoscore = 3

Edit history
 

Gene search

"GENE" or "GENE A123C":

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