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See other EML2 GT Assays ›
SNP ID:
rs750037044
Gene
EML2
Gene Name
Set Membership:
-
Chromosome Location:
Chr.19: 45621629 - 45621629 on Build GRCh38
Polymorphism:
G/A, Transition substitution
Context Sequence [VIC/FAM]:

GCGCCCAGCACCGCCTGTGTGATAC[G/A]GTTCCCACCTGCAGGGTGGCCAGGG

Assay ID C_346868267_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 EML2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
EML2 - echinoderm microtubule associated protein like 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001193268.1 1607 Missense Mutation CGT,TGT R,C 485 NP_001180197.1
NM_001193269.1 1607 Missense Mutation CGT,TGT R,C 431 NP_001180198.1
NM_012155.2 1607 Missense Mutation CGT,TGT R,C 284 NP_036287.1
XM_006723125.2 1607 Missense Mutation CGT,TGT R,C 484 XP_006723188.1
XM_006723126.2 1607 Missense Mutation CGT,TGT R,C 430 XP_006723189.1
XM_011526694.2 1607 Missense Mutation CGT,TGT R,C 453 XP_011524996.1
XM_011526695.2 1607 Missense Mutation CGT,TGT R,C 440 XP_011524997.1
XM_011526698.2 1607 Missense Mutation CGT,TGT R,C 262 XP_011525000.1
XM_011526700.2 1607 Missense Mutation CGT,TGT R,C 168 XP_011525002.1
XM_011526701.2 1607 Missense Mutation CGT,TGT R,C 99 XP_011525003.1
XM_017026550.1 1607 Missense Mutation CGT,TGT R,C 252 XP_016882039.1
XM_017026551.1 1607 Missense Mutation CGT,TGT R,C 485 XP_016882040.1

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