Sample Details for Hap5017887

Hg ID: Hap5017887
GenBank ID: HQ384199.1
Haplogroup: L2a5

Published in: Evolutionary Analyses of Entire Genomes Do Not Support the Association of mtDNA Mutations with Ras/MAPK Pathway Syndromes
Publication Notes: patient45
Details:
Sample source link: http://www.ncbi.nlm.nih.gov/nuccore/HQ384199.1

RSRS Haplotype: 182, 195, 247, 309.1C, 315.1C, 511, 825T, 1737, 2416, 2626, 2758, 2885, 3654, 4312, 4823, 5246A, 5263, 6040C, 6080, 6248, 6497, 6893, 6918, 7146, 7175, 8014, 8206, 8468, 8655, 8723, 9221, 10115, 10664, 10688, 10810, 10915, 11914, 11944, 12285G, 12879, 12967, 13105, 13276, 13506, 13590, 13810, 14088, 14890, 15301, 15758, 16066, 16129, 16182C, 16183C, 16187, 16224, 16230, 16311, 16390

Missing Variants: L2a5:16189

Additional Variants: L2a5:309.1C, 315.1C, 511, 1737, 4823, 5246A, 6080, 6248, 6893, 6918, 8014, 8723, 12285G, 12967, 13810, 14088, 15758, 16066, 16182C, 16183C


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