Product Details

SNP ID

rs78672566

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:179443409 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACACGGCTGCCGCCGCTGCGAGAGG[A/T]GAGGACAGGAAGGCTGGGGCCAAAG

Phenotype

MIM: 612344

Polymorphism

A/T, Transversion 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	1177	Silent Mutation	TCA,TCT	S343S	NP_001106868.1
NM_001113398.1	1177	Silent Mutation	TCA,TCT	S317S	NP_001106869.1
NM_001282725.1	1177	Silent Mutation	TCA,TCT	S317S	NP_001269654.1
NM_152520.4	1177	Silent Mutation	TCA,TCT	S419S	NP_689733.3
XM_011510713.2	1177	Silent Mutation	TCA,TCT	S474S	XP_011509015.1
XM_011510714.2	1177	Silent Mutation	TCA,TCT	S461S	XP_011509016.1
XM_011510715.2	1177	Silent Mutation	TCA,TCT	S447S	XP_011509017.1
XM_011510716.2	1177	Silent Mutation	TCA,TCT	S377S	XP_011509018.1
XM_011510717.2	1177	Silent Mutation	TCA,TCT	S377S	XP_011509019.1
XM_011510719.2	1177	Silent Mutation	TCA,TCT	S357S	XP_011509021.1
XM_011510720.2	1177	Silent Mutation	TCA,TCT	S357S	XP_011509022.1
XM_011510721.2	1177	Silent Mutation	TCA,TCT	S344S	XP_011509023.1
XM_011510723.2	1177	Intron			XP_011509025.1
XM_017003435.1	1177	Silent Mutation	TCA,TCT	S434S	XP_016858924.1
XM_017003436.1	1177	Silent Mutation	TCA,TCT	S357S	XP_016858925.1
XM_017003437.1	1177	Silent Mutation	TCA,TCT	S351S	XP_016858926.1
XM_017003438.1	1177	Silent Mutation	TCA,TCT	S317S	XP_016858927.1
XM_017003439.1	1177	Silent Mutation	TCA,TCT	S317S	XP_016858928.1
XM_017003440.1	1177	Silent Mutation	TCA,TCT	S305S	XP_016858929.1
XM_017003441.1	1177	Intron			XP_016858930.1

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