Product Details

SNP ID

rs77911976

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:55027373 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGACCTACACGAGGTGCAGGAGTG[A/G]TTGGGCCTCCCCTCTCCACTTAAGC

Phenotype

MIM: 616337 MIM: 608126

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SOCS4 PubMed Links

Additional Information

For this assay, SNP(s) [rs77678033] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SOCS4

Gene Name

suppressor of cytokine signaling 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_080867.2	248	UTR 5			NP_543143.1
NM_199421.1	248	UTR 5			NP_955453.1
XM_011536425.1	248	UTR 5			XP_011534727.1
XM_011536426.1	248	UTR 5			XP_011534728.1

Gene

WDHD1

Gene Name

WD repeat and HMG-box DNA binding protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001008396.2	248	Intron			NP_001008397.1
NM_007086.3	248	Intron			NP_009017.1
XM_006720012.2	248	Intron			XP_006720075.1
XM_011536373.2	248	Intron			XP_011534675.1
XM_017020940.1	248	Intron			XP_016876429.1
XM_017020941.1	248	Intron			XP_016876430.1

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