Product Details

SNP ID

rs6561

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.17:27301794 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TTTTTATTTTTCCTTTTAGTGAGAT[C/T]ACGTACTATAGGTGAACTTTTAGCT

Phenotype

MIM: 610091

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIR4522 PubMed Links

Gene Details

Gene

MIR4522

Gene Name

microRNA 4522

There are no transcripts associated with this gene.

Gene

WSB1

Gene Name

WD repeat and SOCS box containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015626.8	462	Missense Mutation	TCA,TTA	S16L	NP_056441.6
NM_134265.2	462	Intron			NP_599027.1
XM_005257963.3	462	Intron			XP_005258020.1
XM_017024433.1	462	Missense Mutation	TCA,TTA	S16L	XP_016879922.1
XM_017024434.1	462	UTR 5			XP_016879923.1
XM_017024435.1	462	UTR 5			XP_016879924.1
XM_017024436.1	462	Intron			XP_016879925.1

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