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PCDH15
NM_033056:c.706-8C>T

Information

Variant Locale INTRON7
PubMed ID (no data)
dbSNP ID (no data)

Call

Variation chr10:56077209: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

6290/8600
European American Alternate Allele Count

3337/4406
African American Alternate Allele Count
1000 Genomes
European

96/132
Utah residents, Northern and Western European ancestry

103/122
Toscani in Italia

98/136
British from England and Scotland

118/162
Finnish from Finland

80/116
Iberian populations in Spain
 
East Asian

32/146
Han Chinese in Beijing, China

21/148
Japanese in Toyko, Japan

46/180
Han Chinese South

33/146
Chinese Dai in Xishuangbanna

80/116
Iberian populations in Spain

39/148
Kinh in Ho Chi Minh City, Vietnam
West African

118/162
Yoruba in Ibadan, Nigeria

41/48
Luhya in Webuye, Kenya
 
Americas

70/98
African Ancestry in Southwest US

83/110
African Caribbean in Barbados

64/116
Mexican Ancestry in Los Angeles, CA

103/140
Puerto Rican in Puerto Rico

69/96
Colombian in Medellin, Colombia

56/94
Peruvian in Lima, Peru
South Asian

83/154
Gujarati Indian in Houston, TX
 
 

Published Data

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

http://vvd.eng.uiowa.edu/variant/893
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