SAMN13396013
External Id
dbGaP
INSDC center name
2019-11-26T21:54:35.797Z
INSDC first public
2024-05-08T13:08:34.700Z
INSDC last update
SRS5854140
INSDC secondary accession
live
INSDC status
Generic
NCBI submission model
Generic.1.0
NCBI submission package
SRS5854140
SRA accession
DNA
analyte type
NCI_FamilialMelanoma
biospecimen repository
C154596
biospecimen repository sample id
Inner Oral Cavity
body site
phs001177
gap_accession
1
gap_consent_code
HMB-MDS
gap_consent_short_name
3719728
gap_sample_id
3071728
gap_subject_id
Buccal
histological type
No
is tumor
Homo sapiens
http://purl.obolibrary.org/obo/NCBITaxon_9606
organism
female
sex
Family/Twin/Trios
study design
Melanoma, Cutaneous Malignant
study disease
Rare Germline Variations in Familial Melanoma
study name
Yes
subject is affected
C154596
submitted sample id
C154596
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