Product Details

SNP ID
rs7175199
Assay Type
Functionally Tested
NCBI dbSNP Submissions
16
Location
Chr.15:49625832 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGTTAGGAGTGGTCTGTCCACTAT[A/G]GTATAAGGCATGTCTGGACATGTTT
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 Intron NP_001138427.1
NM_020234.5 Intron NP_064619.2
XM_011521815.1 Intron XP_011520117.1
XM_017022419.1 Intron XP_016877908.1
XM_017022420.1 Intron XP_016877909.1
XM_017022421.1 Intron XP_016877910.1
XM_017022422.1 Intron XP_016877911.1
XM_017022423.1 Intron XP_016877912.1
XM_017022424.1 Intron XP_016877913.1
XM_017022425.1 Intron XP_016877914.1
XM_017022426.1 Intron XP_016877915.1
XM_017022427.1 Intron XP_016877916.1
XM_017022428.1 Intron XP_016877917.1
XM_017022429.1 Intron XP_016877918.1
XM_017022430.1 Intron XP_016877919.1
XM_017022431.1 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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