Product Details

SNP ID

rs138426884

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:16922705 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTGCCAGGAGAAAGGCTTGGGC[A/G]CGCGGGACCTGGCCCAGGACGCTCA

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	149	Missense Mutation	ACG,GCG	T35A	NP_055490.4
XM_006711058.3	149	Intron			XP_006711121.1
XM_011542468.1	149	Missense Mutation	ACG,GCG	T37A	XP_011540770.1
XM_011542470.2	149	Missense Mutation	ACG,GCG	T37A	XP_011540772.1
XM_017002913.1	149	Missense Mutation	ACG,GCG	T37A	XP_016858402.1
XM_017002914.1	149	Missense Mutation	ACG,GCG	T37A	XP_016858403.1
XM_017002915.1	149	Missense Mutation	ACG,GCG	T37A	XP_016858404.1

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