Product Details

SNP ID

rs11539522

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:49625193 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTCTCTCAATCCACCTATATTTC[C/T]CAAACGAAGTGAAGAAAATAGTTCA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DTWD1 PubMed Links

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	222	Missense Mutation	CCC,CTC	P9L	NP_001138427.1
NM_020234.5	222	Missense Mutation	CCC,CTC	P9L	NP_064619.2
XM_011521815.1	222	Missense Mutation	CCC,CTC	P9L	XP_011520117.1
XM_017022419.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877908.1
XM_017022420.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877909.1
XM_017022421.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877910.1
XM_017022422.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877911.1
XM_017022423.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877912.1
XM_017022424.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877913.1
XM_017022425.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877914.1
XM_017022426.1	222	Missense Mutation	CCC,CTC	P9L	XP_016877915.1
XM_017022427.1	222	UTR 5			XP_016877916.1
XM_017022428.1	222	UTR 5			XP_016877917.1
XM_017022429.1	222	UTR 5			XP_016877918.1
XM_017022430.1	222	UTR 5			XP_016877919.1
XM_017022431.1	222	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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