Product Details

SNP ID

rs9963473

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:35369591 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATGAAGGATATTGGAAACATTGCAA[A/T]GCAGTTCTATGCCTAAAGAAGTCTT

Phenotype

MIM: 609600

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

ZNF396 PubMed Links

Gene Details

Gene

ZNF396

Gene Name

zinc finger protein 396

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001322286.1	764	Missense Mutation	CAT,CTT	H211L	NP_001309215.1
NM_001322290.1	764	Missense Mutation	CAT,CTT	H211L	NP_001309219.1
NM_001322291.1	764	Intron			NP_001309220.1
NM_145756.2	764	Missense Mutation	CAT,CTT	H211L	NP_665699.1
XM_006722432.3	764	Missense Mutation	CAT,CTT	H211L	XP_006722495.1
XM_017025687.1	764	Missense Mutation	CAT,CTT	H211L	XP_016881176.1
XM_017025688.1	764	Missense Mutation	CAT,CTT	H211L	XP_016881177.1
XM_017025689.1	764	Missense Mutation	CAT,CTT	H211L	XP_016881178.1

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