Product Details

SNP ID
rs17756631
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:27675205 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATGAAAACACCGGAAAGAACATCCA[C/T]TGGATCTGAAAAGCAACAAGCTCTT
Phenotype
MIM: 601332
Polymorphism
C/T, Transition 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 1308 UTR 3 NP_001229631.1
NM_173576.2 1308 UTR 3 NP_775847.2
XM_017016105.1 1308 UTR 3 XP_016871594.1
XM_017016106.1 1308 UTR 3 XP_016871595.1
XM_017016107.1 1308 Intron XP_016871596.1
XM_017016108.1 1308 UTR 3 XP_016871597.1

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