Product Details

SNP ID
rs61740454
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67252687 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCAGGCACCTTCTTCCTCTTCCT[C/G]CTGCCTCCTATTGTGTTGGACTCAG
Phenotype
MIM: 606881 MIM: 600477
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FHOD1 PubMed Links

Gene Details

Gene
FHOD1
Gene Name
formin homology 2 domain containing 1
There are no transcripts associated with this gene.

Gene
SLC9A5
Gene Name
solute carrier family 9 member A5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323971.1 1799 Silent Mutation CTC,CTG L111L NP_001310900.1
NM_001323972.1 1799 Intron NP_001310901.1
NM_001323973.1 1799 Silent Mutation CTC,CTG L111L NP_001310902.1
NM_001323974.1 1799 UTR 5 NP_001310903.1
NM_001323975.1 1799 UTR 5 NP_001310904.1
NM_004594.2 1799 Silent Mutation CTC,CTG L111L NP_004585.1
XM_017023594.1 1799 Silent Mutation CTC,CTG L111L XP_016879083.1

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