Product Details

SNP ID

rs6460207

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:64888699 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCAAAGTCTTCGGGGTGAGAGGTCC[C/G]GCTCCTGGAGGACAGCGGGATGGGA

Phenotype

MIM: 604756

Polymorphism

C/G, 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	400	Missense Mutation	CGG,GGG	R177G	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	400	Intron			NP_066971.2
XM_011515746.2	400	Intron			XP_011514048.1
XM_017011688.1	400	Intron			XP_016867177.1
XM_017011689.1	400	UTR 5			XP_016867178.1
XM_017011690.1	400	UTR 5			XP_016867179.1
XM_017011691.1	400	UTR 5			XP_016867180.1
XM_017011692.1	400	UTR 5			XP_016867181.1
XM_017011693.1	400	Intron			XP_016867182.1
XM_017011694.1	400	Intron			XP_016867183.1
XM_017011695.1	400	Intron			XP_016867184.1
XM_017011696.1	400	Intron			XP_016867185.1
XM_017011697.1	400	UTR 5			XP_016867186.1
XM_017011698.1	400	Intron			XP_016867187.1

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