Product Details

SNP ID
rs147020374
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:27675552 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTTATTGGATCCGTTTTCCAGAG[A/T]GTCTGTAAAGAAAAGCAAAAATTCA
Phenotype
MIM: 601332
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
MKX PubMed Links

Gene Details

Gene
MKX
Gene Name
mohawk homeobox
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242702.1 1066 Missense Mutation ACT,TCT T281S NP_001229631.1
NM_173576.2 1066 Missense Mutation ACT,TCT T281S NP_775847.2
XM_017016105.1 1066 Missense Mutation ACT,TCT T281S XP_016871594.1
XM_017016106.1 1066 Missense Mutation ACT,TCT T281S XP_016871595.1
XM_017016107.1 1066 Intron XP_016871596.1
XM_017016108.1 1066 Missense Mutation ACT,TCT T281S XP_016871597.1

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