Sample Details for Hap5009157

Hg ID: Hap5009157
GenBank ID: EF661007.1
Haplogroup: V23

Published in: Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors
Publication Notes: PA_EU_IT_0093
Details:
Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/EF661007.1

RSRS Haplotype: 72, 73, 146, 152, 195, 247, 309.1C, 315.1C, 769, 825T, 1018, 2758, 2885, 3594, 4104, 4312, 4580, 6734, 7146, 7256, 7521, 8468, 8655, 8701, 9540, 10398, 10664, 10688, 10810, 10873, 10915, 11719, 11914, 12705, 13042R, 13105, 13276, 13506, 13650, 14766, 15904, 16129, 16187, 16189, 16223, 16230, 16278, 16298, 16311

Missing Variants: none

Additional Variants: V23:309.1C, 315.1C, 13042R


Last Updated: 2016/06/29 10:51:00 PM