Product Details

SNP ID
rs11539519
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:49625204 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCCACCTATATTTCTCAAACGAAGT[A/G]AAGAAAATAGTTCAAAATTTGTGGA
Phenotype
Polymorphism
A/G, 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_001144955.1 233 Missense Mutation AAA,GAA K13E NP_001138427.1
NM_020234.5 233 Missense Mutation AAA,GAA K13E NP_064619.2
XM_011521815.1 233 Missense Mutation AAA,GAA K13E XP_011520117.1
XM_017022419.1 233 Missense Mutation AAA,GAA K13E XP_016877908.1
XM_017022420.1 233 Missense Mutation AAA,GAA K13E XP_016877909.1
XM_017022421.1 233 Missense Mutation AAA,GAA K13E XP_016877910.1
XM_017022422.1 233 Missense Mutation AAA,GAA K13E XP_016877911.1
XM_017022423.1 233 Missense Mutation AAA,GAA K13E XP_016877912.1
XM_017022424.1 233 Missense Mutation AAA,GAA K13E XP_016877913.1
XM_017022425.1 233 Missense Mutation AAA,GAA K13E XP_016877914.1
XM_017022426.1 233 Missense Mutation AAA,GAA K13E XP_016877915.1
XM_017022427.1 233 UTR 5 XP_016877916.1
XM_017022428.1 233 UTR 5 XP_016877917.1
XM_017022429.1 233 UTR 5 XP_016877918.1
XM_017022430.1 233 UTR 5 XP_016877919.1
XM_017022431.1 233 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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