Sample Details for Hap5009161

Hg ID: Hap5009161
GenBank ID: EF661011.1
Haplogroup: N1b1a2

Published in: Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors
Publication Notes: PA_EU_IT_0097
Details:
Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/EF661011.1

RSRS Haplotype: 146, 152, 195, 247, 310, 315.1C, 769, 825T, 1018, 1598, 1703, 1719, 2639, 2758, 2885, 3594, 3921A, 4104, 4312, 4904, 4960, 5471, 7146, 7256, 7521, 8251, 8468, 8472, 8655, 8701, 8836, 9335, 9540, 10238, 10398, 10664, 10688, 10810, 10873, 10915, 11362, 11914, 12501, 12797, 12822, 13105, 13276, 13506, 13650, 14470, 16129, 16145, 16176G, 16187, 16189, 16230, 16278, 16311, 16390

Missing Variants: none

Additional Variants: N1b1a2:152, 310, 315.1C, 12797, 14470


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