Product Details

SNP ID
rs139763565
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:16924335 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGTCCCTTGCCAGTCCTGCTGCC[A/G]GCCACAGAGATGGCATCGCTGCTGT
Phenotype
MIM: 615776
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CROCC PubMed Links

Gene Details

Gene
CROCC
Gene Name
ciliary rootlet coiled-coil, rootletin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014675.4 67 Silent Mutation CCA,CCG P69P NP_055490.4
XM_006711058.3 67 UTR 5 XP_006711121.1
XM_011542468.1 67 Silent Mutation CCA,CCG P71P XP_011540770.1
XM_011542470.2 67 Silent Mutation CCA,CCG P71P XP_011540772.1
XM_017002913.1 67 Silent Mutation CCA,CCG P71P XP_016858402.1
XM_017002914.1 67 Silent Mutation CCA,CCG P71P XP_016858403.1
XM_017002915.1 67 Silent Mutation CCA,CCG P71P XP_016858404.1

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