ALFRED detailed record information
Synonyms: T2 ; rs6313 ;
|Fst||Avg Het||# Populations Typed|
Frequency Display Formats:
External Resources: dbSNP rs# Record PharmGKB Variant Information Record
References: See References
Polymorphism Description: A T/C SNP altering a MspI restriction site. This polymorphism is located at position 102. Both allele (TCT) and allele (TCC) encode for a serine at amino acid #34.
|Allele Name||Allele Symbol||Description|
- Chakrabarti CS, Roy M, Sengupta NK, Lalthantluanga R, Majumder PP.
"Genetic relationships among some tribal groups inhabiting the north-eastern, eastern and sub-Himalayan regions of India". Ann Hum Genet 66:361-368. (2002) Online citation.
- Jorde LB, Bamshad MJ, Watkins WS, Zenger R, Fraley AE, Krakowiak PA, Carpenter KD, Soodyall H, Jenkins T, Rogers AR. "Origins and affinities of modern humans: a comparison of mitochondrial and nuclear genetic data.". Am. J. Hum. Genet. 57:523-538. (1995) Online citation.
- Warren JT Jr, Peacock ML, Rodriguez LC, Fink JK. "An MspI polymorphism in the hyman serotonin receptor gene (HTR2): detection by DGGE and RFLP analysis". Hum. Mol. Genet. 2:338. (1993) Online citation.
© 2018 Kenneth K Kidd, Yale University. All rights reserved. The full Copyright Notification is also available.
Originally prototyped by Michael Osier with the aid of Kei Cheung
Upgrades and maintenance since 2002 by Haseena Rajeevan