Product Details

SNP ID
rs186913032
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:6240314 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCCTTTCGCATTGCCAAGCTGATG[C/G]TTTACATTTTTGTCGTCATCCATTG
Phenotype
MIM: 609472
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CNGA4 PubMed Links

Gene Details

Gene
CNGA4
Gene Name
cyclic nucleotide gated channel alpha 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001037329.3 542 Missense Mutation CTT,GTT L174V NP_001032406.1
XM_017017217.1 542 Missense Mutation CTT,GTT L174V XP_016872706.1
XM_017017218.1 542 Missense Mutation CTT,GTT L134V XP_016872707.1
XM_017017219.1 542 Missense Mutation CTT,GTT L134V XP_016872708.1
Gene
FAM160A2
Gene Name
family with sequence similarity 160 member A2
There are no transcripts associated with this gene.

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