Product Details

SNP ID

rs184025907

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:72074335 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTGCAAATGGCTATGTGGAGCACT[C/T]GTTTCGCTACCAGTGTAAGAACTAC

Phenotype

MIM: 140210

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HPR PubMed Links

Additional Information

For this assay, SNP(s) [rs7202157,rs7202158] are located under a primer 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

HPR

Gene Name

haptoglobin-related protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020995.3	173	Missense Mutation	TCG,TTG	S48L	NP_066275.3

Gene

TXNL4B

Gene Name

thioredoxin like 4B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142317.1	173	Intron			NP_001135789.1
NM_001142318.1	173	Intron			NP_001135790.1
NM_001324354.1	173	Intron			NP_001311283.1
NM_001324355.1	173	Intron			NP_001311284.1
NM_017853.2	173	Intron			NP_060323.1
XM_017023377.1	173	Intron			XP_016878866.1

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