Product Details

SNP ID
rs201706236
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:35155567 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCCACAGATGTCGCCCTCTGGTC[A/G]CCTGTGTCTTCTCACCATCGTTGGC
Phenotype
MIM: 606669 MIM: 606684
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FXYD5 PubMed Links

Gene Details

Gene
FXYD5
Gene Name
FXYD domain containing ion transport regulator 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001164605.1 105 Missense Mutation CAC,CGC H6R NP_001158077.1
NM_001320912.1 105 Missense Mutation CAC,CGC H6R NP_001307841.1
NM_001320913.1 105 Missense Mutation CAC,CGC H6R NP_001307842.1
NM_014164.5 105 Missense Mutation CAC,CGC H6R NP_054883.3
NM_144779.2 105 Missense Mutation CAC,CGC H6R NP_659003.1
Gene
FXYD7
Gene Name
FXYD domain containing ion transport regulator 7
There are no transcripts associated with this gene.

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