SAMN13396548
External Id
dbGaP
INSDC center name
2019-11-26T21:55:02.657Z
INSDC first public
2024-05-04T04:30:17.803Z
INSDC last update
SRS5856409
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5856409
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
139403
biospecimen repository sample id
Inner Oral Cavity
body site
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3718778
gap_sample_id
3070778
gap_subject_id
Buccal
http://purl.obolibrary.org/obo/UBERON_0003679
histological type
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
http://purl.obolibrary.org/obo/PATO_0000383
sex
Family/Twin/Trios
study design
Melanoma, Cutaneous Malignant
study disease
Rare Germline Variations in Familial Melanoma
study name
Yes
subject is affected
139403
submitted sample id
139403
submitted subject id
NCI_FamilialMelanoma
submitter handle
Non-tumor DNA sample from Inner Oral Cavity of a human female participant in the dbGaP study Rare Germline Variations in Familial Melanoma
title