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NM_000180:p.Pro1099Pro

GUCY2D
NM_000180:c.3297G>A

Information

Variant Locale EXON19
PubMed ID (no data)
dbSNP ID (no data)

Call

Variation chr17:7919833:G>A
Pathogenicity Benign
Phenotype

Interpretation

In Silico Computational

SIFT Polyphen-2 LRT MutationTaster PhyloP GERP++
Unknown Unknown Unknown Unknown Unknown Unknown

Variant Frequencies

OtoSCOPE™

(No data)
Alternate Allele Count
Exome Variant Server

187/8384
European American Alternate Allele Count

37/4266
African American Alternate Allele Count
1000 Genomes
European

1/122
Utah residents, Northern and Western European ancestry

1/114
Toscani in Italia

1/128
British from England and Scotland

5/152
Finnish from Finland

2/112
Iberian populations in Spain
 
East Asian

(No data)
Han Chinese in Beijing, China

(No data)
Japanese in Toyko, Japan

(No data)
Han Chinese South

(No data)
Chinese Dai in Xishuangbanna

2/112
Iberian populations in Spain

(No data)
Kinh in Ho Chi Minh City, Vietnam
West African

1/152
Yoruba in Ibadan, Nigeria

(No data)
Luhya in Webuye, Kenya
 
Americas

(No data)
African Ancestry in Southwest US

1/108
African Caribbean in Barbados

(No data)
Mexican Ancestry in Los Angeles, CA

(No data)
Puerto Rican in Puerto Rico

5/92
Colombian in Medellin, Colombia

2/90
Peruvian in Lima, Peru
South Asian

1/142
Gujarati Indian in Houston, TX
 
 

Published Data

Manual curation in progress. Record generated from: ESP6500, 1000 Genomes.

http://vvd.eng.uiowa.edu/variant/1581
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