Product Details

SNP ID

rs145623392

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:179444888 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGGTAAACTTACTGCTAGAATACT[C/T]GGGCTCCGCTGGAGTTTGTTGTAAG

Phenotype

MIM: 612344

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF385B PubMed Links

Gene Details

Gene

ZNF385B

Gene Name

zinc finger protein 385B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001113397.1	1105	Silent Mutation	CCA,CCG	P319P	NP_001106868.1
NM_001113398.1	1105	Silent Mutation	CCA,CCG	P293P	NP_001106869.1
NM_001282725.1	1105	Silent Mutation	CCA,CCG	P293P	NP_001269654.1
NM_152520.4	1105	Silent Mutation	CCA,CCG	P395P	NP_689733.3
XM_011510713.2	1105	Silent Mutation	CCA,CCG	P450P	XP_011509015.1
XM_011510714.2	1105	Silent Mutation	CCA,CCG	P437P	XP_011509016.1
XM_011510715.2	1105	Silent Mutation	CCA,CCG	P423P	XP_011509017.1
XM_011510716.2	1105	Silent Mutation	CCA,CCG	P353P	XP_011509018.1
XM_011510717.2	1105	Silent Mutation	CCA,CCG	P353P	XP_011509019.1
XM_011510719.2	1105	Silent Mutation	CCA,CCG	P333P	XP_011509021.1
XM_011510720.2	1105	Silent Mutation	CCA,CCG	P333P	XP_011509022.1
XM_011510721.2	1105	Silent Mutation	CCA,CCG	P320P	XP_011509023.1
XM_011510723.2	1105	Intron			XP_011509025.1
XM_017003435.1	1105	Silent Mutation	CCA,CCG	P410P	XP_016858924.1
XM_017003436.1	1105	Silent Mutation	CCA,CCG	P333P	XP_016858925.1
XM_017003437.1	1105	Silent Mutation	CCA,CCG	P327P	XP_016858926.1
XM_017003438.1	1105	Silent Mutation	CCA,CCG	P293P	XP_016858927.1
XM_017003439.1	1105	Silent Mutation	CCA,CCG	P293P	XP_016858928.1
XM_017003440.1	1105	Silent Mutation	CCA,CCG	P281P	XP_016858929.1
XM_017003441.1	1105	Intron			XP_016858930.1

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