Product Details

SNP ID

rs182054421

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:9757773 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTCTTAAATGGGTACTAAGGCCC[A/G]AGGATTGAGTGAAAGCTTTCCCACA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ZNF846 PubMed Links

Gene Details

Gene

ZNF846

Gene Name

zinc finger protein 846

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077624.1	2275	Missense Mutation	TCG,TTG	S435L	NP_001071092.1
XM_005259772.3	2275	Missense Mutation	TCG,TTG	S435L	XP_005259829.1
XM_005259773.4	2275	Missense Mutation	TCG,TTG	S434L	XP_005259830.1
XM_005259775.3	2275	Missense Mutation	TCG,TTG	S434L	XP_005259832.1
XM_006722658.3	2275	Intron			XP_006722721.1
XM_011527717.2	2275	Missense Mutation	TCG,TTG	S435L	XP_011526019.1
XM_011527718.2	2275	Missense Mutation	TCG,TTG	S434L	XP_011526020.1
XM_011527719.2	2275	Missense Mutation	TCG,TTG	S399L	XP_011526021.1
XM_011527720.2	2275	Missense Mutation	TCG,TTG	S399L	XP_011526022.1
XM_011527721.2	2275	Missense Mutation	TCG,TTG	S378L	XP_011526023.1
XM_017026404.1	2275	Missense Mutation	TCG,TTG	S421L	XP_016881893.1
XM_017026405.1	2275	Missense Mutation	TCG,TTG	S306L	XP_016881894.1
XM_017026406.1	2275	Missense Mutation	TCG,TTG	S306L	XP_016881895.1
XM_017026407.1	2275	Intron			XP_016881896.1
XM_017026408.1	2275	Intron			XP_016881897.1

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