Product Details

SNP ID

rs884103

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:64889493 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCCCGCGGGACGCCAGGTTCCCGG[A/T]TTCTTCTAGGTCGCCCTGGTTCCTG

Phenotype

MIM: 604756

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

LOC441239 PubMed Links

Gene Details

Gene

LOC441239

Gene Name

uncharacterized LOC441239

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011516745.2	1194	Missense Mutation	ACC,TCC	T83S	XP_011515047.1

Gene

ZNF273

Gene Name

zinc finger protein 273

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021148.2	1194	Intron			NP_066971.2
XM_011515746.2	1194	Intron			XP_011514048.1
XM_017011688.1	1194	Intron			XP_016867177.1
XM_017011689.1	1194	UTR 5			XP_016867178.1
XM_017011690.1	1194	UTR 5			XP_016867179.1
XM_017011691.1	1194	UTR 5			XP_016867180.1
XM_017011692.1	1194	UTR 5			XP_016867181.1
XM_017011693.1	1194	Intron			XP_016867182.1
XM_017011694.1	1194	Intron			XP_016867183.1
XM_017011695.1	1194	Intron			XP_016867184.1
XM_017011696.1	1194	Intron			XP_016867185.1
XM_017011697.1	1194	UTR 5			XP_016867186.1
XM_017011698.1	1194	Intron			XP_016867187.1

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