Product Details
- SNP ID
-
rs142654959
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:49625421 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAAAATGTACCTATTGAACAGATTC[C/T]ACTTGTGAAGGTTAGTAAGAAATTT
- 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 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
NP_001138427.1 |
NM_020234.5 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
NP_064619.2 |
XM_011521815.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_011520117.1 |
XM_017022419.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877908.1 |
XM_017022420.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877909.1 |
XM_017022421.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877910.1 |
XM_017022422.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877911.1 |
XM_017022423.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877912.1 |
XM_017022424.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877913.1 |
XM_017022425.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877914.1 |
XM_017022426.1 |
450 |
Missense Mutation |
CCA,CTA |
P85L |
XP_016877915.1 |
XM_017022427.1 |
450 |
UTR 5 |
|
|
XP_016877916.1 |
XM_017022428.1 |
450 |
UTR 5 |
|
|
XP_016877917.1 |
XM_017022429.1 |
450 |
UTR 5 |
|
|
XP_016877918.1 |
XM_017022430.1 |
450 |
UTR 5 |
|
|
XP_016877919.1 |
XM_017022431.1 |
450 |
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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