C___8770904_10

• SNP ID: rs779168
• Gene: ZNF385D
• Gene Name: zinc finger protein 385D
• Set Membership: > HapMap
• Chromosome Location: Chr.3: 22063903 - 22063903 on Build GRCh38
• Polymorphism: C/G, Transversion substitution
• Context Sequence [VIC/FAM]:

  AGGCCTTTGTTTTGACAGCAGGACA[C/G]CTTGATTTTCCATCTGCCCAGTCTT

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:
Literature Links:	ZNF385D PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome	Applied Biosystems^®	HapMap
Global C (0.36) (0.64)	Caucasian - Not Available	CEPH (CEU) C (0.31) (0.69)
EAS C (0.49) (0.51)	African American - Not Available	YRI (Yoruba) C (0.13) (0.87)
SAS C (0.43) (0.57)	Chinese - Not Available	JPT (Japanese) G (0.42) (0.58)
AFR C (0.13) (0.87)	Japanese - Not Available	CHB (Han Chinese) C (0.47) (0.53)
EUR C (0.39) (0.61)
AMR C (0.47) (0.53)

ZNF385D - zinc finger protein 385D
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_024697.2		Intron			NP_078973.1
XM_011534122.1		Intron			XP_011532424.1
XM_011534123.2		Intron			XP_011532425.1
XM_011534124.2		Intron			XP_011532426.1
XM_017007191.1		Intron			XP_016862680.1
XM_017007192.1		Intron			XP_016862681.1
XM_017007193.1		Intron			XP_016862682.1
XM_017007194.1		Intron			XP_016862683.1
XM_017007195.1		Intron			XP_016862684.1
XM_017007196.1		Intron			XP_016862685.1
XM_017007197.1		Intron			XP_016862686.1
XM_017007198.1		Intron			XP_016862687.1
XM_017007199.1		Intron			XP_016862688.1
XM_017007200.1		Intron			XP_016862689.1
XM_017007201.1		Intron			XP_016862690.1
XM_017007202.1		Intron			XP_016862691.1
XM_017007203.1		Intron			XP_016862692.1

More Information

• Set Membership: HapMap

Gene Ontology Categories:

Process(es)

intrinsic apoptotic signaling pathway by p53 class mediator

Function(s)

p53 binding
RNA binding
zinc ion binding