Product Details

SNP ID

rs182263854

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:49625202 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATCCACCTATATTTCTCAAACGAA[A/G]TGAAGAAAATAGTTCAAAATTTGTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DTWD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs11539519] 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

DTWD1

Gene Name

DTW domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001144955.1	231	Missense Mutation	AAT,AGT	N12S	NP_001138427.1
NM_020234.5	231	Missense Mutation	AAT,AGT	N12S	NP_064619.2
XM_011521815.1	231	Missense Mutation	AAT,AGT	N12S	XP_011520117.1
XM_017022419.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877908.1
XM_017022420.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877909.1
XM_017022421.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877910.1
XM_017022422.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877911.1
XM_017022423.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877912.1
XM_017022424.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877913.1
XM_017022425.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877914.1
XM_017022426.1	231	Missense Mutation	AAT,AGT	N12S	XP_016877915.1
XM_017022427.1	231	UTR 5			XP_016877916.1
XM_017022428.1	231	UTR 5			XP_016877917.1
XM_017022429.1	231	UTR 5			XP_016877918.1
XM_017022430.1	231	UTR 5			XP_016877919.1
XM_017022431.1	231	Intron			XP_016877920.1

Gene

FAM227B

Gene Name

family with sequence similarity 227 member B

There are no transcripts associated with this gene.

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