I1583

FASTA

Metadata

Reference

Data

identifier I1583
alternative_identifiers ['L14-200']
country Turkey
continent Asia
region Anatolia
culture Anatolia_Neolithic
epoch Neolithic
group NENE
comment -
latitude 40.29999923706055
longitude 29.56999969482422
sex M
site Barcın, Marmara Region, Northwest Anatolia
site_detail -
mt_hg K1a2
ychr_hg G2a2a1a2a
year_from -6426
year_to -6236
date_detail 6426-6236 calBCE (7460±50 BP, Poz-82231)
bp 7460±50
c14_lab_code Poz-82231
c14_sample_tag True
c14_layer_tag -
avg_coverage -
sequence_source bam
reference Mathieson et al. 2015. Genome-wide patterns of selection in 230 ancient Eurasians. Nature, 528(7583), 499-503. (link)
data_link https://www.ebi.ac.uk/ena/data/view/PRJEB11450
ychr_snps ['G2a2:CTS4367:15615340C->G', 'G2a:CTS6630:17022002C->T', 'G2a:F2529:17571517A->G', 'G2a:F3088:20813445G->A', 'G2a:F4086:7727677C->T', 'G2a:L31:14028148C->A', 'G2a:M3393:21493984G->T', 'G2a:M3397:21605685G->C', 'G2a:M3408:22109159G->C', 'G2a:P15:23244026C->T', 'G2a:PF3141:23973594T->G', 'G2:CTS1900:14116322T->A', 'G2:CTS2406:14294068C->T', 'G2:CTS10089:19248446G->A', 'G2:F1239:8482393C->T', 'G2:F1294:8545324T->A', 'G2:F1393:8719593G->A', 'G2:F3070:19493301A->G', 'G2:F3198:21401188G->T', 'G2:F3220:21637589G->C', 'G2:F3536:23768744C->T', 'G2:L89:7978725C->T', 'G2:P287:22072097G->T', 'G:CTS34:2681740G->A', 'G:CTS175:2785630A->T', 'G:CTS1013:7145960C->T', 'G:CTS1283:7309873T->G', 'G:CTS2271:14243137C->T', 'G:CTS2357:14273557C->T', 'G:CTS2506:14333087C->A', 'G:CTS4238:15504804C->T', 'G:CTS4761:15802681C->T', 'G:CTS4887:15888550C->T', 'G:CTS5699:16439267G->A', 'G:CTS6957:17210745C->T', 'G:CTS7092:17281783G->A', 'G:CTS7674:17610571G->A', 'G:CTS8023:17798903T->C', 'G:CTS9011:18615020A->T', 'G:CTS9593:18979775T->A', 'G:CTS10026:19215139A->T', 'G:CTS10723:22730922C->G', 'G:CTS10945:22848965A->G', 'G:CTS11228:23023554C->A', 'G:CTS11331:23074190A->G', 'G:CTS11529:23151673T->C', 'G:CTS11911:23346582A->C', 'G:CTS13035:28783924C->A', 'G:F1131:8240725C->T', 'G:F1383:8700380C->T', 'G:F1551:9448354A->G', 'G:F2076:16185081A->G', 'G:L116:14989721C->G', 'G:L382:14469411C->A', 'G:L522:17533325A->C', 'G:L770:2863466A->T', 'G:L837:17853245A->G', 'G:M3258:7992031T->C', 'G:M3432:23578115C->G', 'G:M3450:6931141C->G', 'G:M3468:7744050T->C', 'G:M3472:7899682T->C', 'G:M3473:7927218C->T', 'G:M3474:7930724C->A', 'G:M3479:8231862G->C', 'G:M3480:8327892T->A', 'G:M3482:8454233G->A', 'G:M3485:8563874C->T', 'G:M3486:8600158A->T', 'G:M3593:21648433C->G', 'G:M3597:21865624G->A', 'G:M3599:21939157G->A', 'G:M3609:22651339C->T', 'G:M3628:23793740C->A', 'G:P257:14432928G->A', 'G:PF2918:13679469G->A', 'G:PF2920:13824120T->G', 'G:PF2952:14577177G->A', 'G:PF3045:20823823C->T', 'G:PF3134:15275200C->G', 'G:S1435:13658486C->Ghet', 'G:U21:15204710A->C', 'G:Z3262:13676268G->A', 'G2a:Z3240:10060449A->G', 'G2:CTS4264:15528792T->C', 'G2:CTS4703:15776024C->T', 'G2:CTS6316:16817402C->T', 'G2:CTS6742:17088129G->C', 'G2:CTS9885:19119067C->T', 'G2:F1189:8427005A->G', 'G2:F1647:9907842G->T', 'G2:F2319:16903051A->T', 'G2:F3226:21663882C->A', 'G2:L156:17174741A->T', 'G2:M3465:7571775G->T', 'G2:M3493:9443697G->A', 'G2:PF2909:13205148A->G', 'G2:PF3119:23739606G->T', 'G2:Y380:28799209T->Chet', 'G:CTS373:6716150T->C', 'G:CTS995:7132348G->C', 'G:CTS1612:13987230A->G', 'G:CTS2120:14188094G->T', 'G:CTS2136:14195292A->G', 'G:CTS2215:14220356G->A', 'G:CTS2517:14338503C->T', 'G:CTS4101:15397649A->G', 'G:CTS4523:15693336G->A', 'G:CTS4749:15797043A->G', 'G:CTS5317:16203361G->C', 'G:CTS5414:16261165C->T', 'G:CTS5504:16325291T->C', 'G:CTS5640:16408569G->A', 'G:CTS6483:16929270C->T', 'G:CTS9710:19033112G->A', 'G:CTS9894:19124322A->T', 'G:CTS10721:22729194C->T', 'G:CTS11294:23059496G->A', 'G:CTS11907:23343857C->G', 'G:L154:8614138T->G', 'G:L402:15204708T->G', 'G:M3264:8318375G->T', 'G:M3266:8422993T->A', 'G:M3274:8865637G->A', 'G:M3464:7537950C->T', 'G:M3466:7614386G->A', 'G:M3470:7830068T->C', 'G:M3471:7840218C->A', 'G:M3481:8387539G->A', 'G:M3580:21162869C->G', 'G:M3582:21334507G->T', 'G:M3585:21412501G->A', 'G:M3586:21447363A->G', 'G:M3627:23782951G->A', 'G:Page94:2846401C->T', 'G:PF2836:6478903G->A', 'G:PF2956:14993358A->G', 'G2a:CTS6026:16620480C->T', 'G2a:CTS6753:17090976C->T', 'G2a:F1980:15660640C->T', 'G2:CTS4242:15507383T->C', 'G2:CTS5666:16424034C->T', 'G:CTS1010:7143549C->T', 'G:CTS4479:15667235G->A', 'G:CTS5757:16469840A->G', 'G:CTS9707:19030998C->A', 'G:CTS10706:22714204G->T', 'G:CTS11400:23095144A->G', 'G:M3477:8121059G->A', 'G:M3487:8602816G->C', 'G:M3595:21671839C->T', 'G2a2a1a2a:PF3237:17017831G->A', 'G2a2a1a2a:PF3238:17256431G->A', 'G2a2a1a2:L91:21645555G->C', 'G2a2a1:PF3170:18090604G->A', 'G2a2a:PF3147:7738069G->A', 'G2a2a:PF3159:14815695C->G', 'G2a2a:PF3181:21808944C->A', 'G2a2a:PF3184:22576860C->T', 'G2a2a:PF3185:22894488C->T', 'G:CTS827:7038432C->G', 'G2a2a1a2:PF3233:8895958T->C', 'G2a2a1:PF3155:14006343T->C', 'G2a2a1:PF3160:14926732C->T', 'G2a2a1:S11769:8648696C->T', 'G2a2a:PF3149:7943188A->G', 'G2a2a:PF3175:18962113C->T', 'G2a2a:Z6178:7245721G->A', 'G:S8863:4179056G->A', 'G2a2a1a2:S19852:17531217C->T', 'G2a2a1a:PF3177:21327198C->T', 'G2a2a1:FGC2268:22120867G->A', 'G2a2a1:S11510:8471941G->A', 'G2a2a1:S15710:14254785T->G', 'G2a2a1:S17801:15998373A->G', 'G2a2a:PF3150:8476569T->C', 'G2a2a:PF3151:9785736A->G', 'G2a:CTS1879:14108344G->A', 'G2a:CTS9318:18819146T->A', 'G2a:CTS11463:23122426G->A', 'G2:CTS4136:15421357G->A', 'G2:CTS4413:15635425T->Chet', 'G2:CTS11196:23005701T->A', 'G2:F3344:22697266G->Ahet', 'G2:M3579:21147058A->Ghet', 'G:CTS282:2871867A->G', 'G:CTS692:6955839A->Ghet', 'G:CTS2125:14190447A->Ghet', 'G:CTS2251:14235140C->Thet', 'G:CTS5658:16419934T->C', 'G:CTS6073:16651032G->A', 'G:CTS7269:17393643T->Chet', 'G:CTS10393:19434150G->T', 'G:CTS12654:28658660G->Thet', 'G:M3248:7565637G->A', 'G:M3257:7991847G->A', 'G:M3476:8064458A->G', 'G:M3490:8742700A->G', 'G:PF2901:9523592C->A']
mitopathos [{'allele': '10398G', 'position': 10398, 'status': 'Reported / lineage L & M marker / also hg IJK', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-ND3'], 'diseases': ['PD protective factor / longevity / altered cell pH / metabolic syndrome / breast cancer risk / Leigh Syndrome risk / ADHD / cognitive decline / SCA2 age of onset / Fuchs endothelial corneal dystrophy']}, {'allele': '11467G', 'position': 11467, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-ND4'], 'diseases': ['Altered brain pH / sCJD patients']}, {'allele': '12308G', 'position': 12308, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '+', 'locus': ['MT-TL2'], 'diseases': ['CPEO / Stroke / CM / Breast & Renal & Prostate Cancer Risk / Altered brain pH /sCJD']}, {'allele': '12372A', 'position': 12372, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-ND5'], 'diseases': ['Altered brain pH / sCJD patients']}, {'allele': '16093C', 'position': 16093, 'status': 'Reported', 'homoplasmy': '-', 'heteroplasmy': '+', 'locus': ['MT-CR'], 'diseases': ['Cyclic Vomiting Syndrome']}, {'allele': '310C', 'position': 310, 'status': 'Reported', 'homoplasmy': '<NA>', 'heteroplasmy': '<NA>', 'locus': ['MT-CR'], 'diseases': ['Possible protective factor for normal tension glaucoma']}, {'allele': '7023A', 'position': 7023, 'status': 'Reported', 'homoplasmy': '-', 'heteroplasmy': '+', 'locus': ['MT-CO1'], 'diseases': ['MELAS-like syndrome']}, {'allele': '9055A', 'position': 9055, 'status': 'Reported', 'homoplasmy': '+', 'heteroplasmy': '-', 'locus': ['MT-ATP6'], 'diseases': ['PD protective factor']}]