Product Details

SNP ID
rs202095674
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:157148326 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCTCAAAGGAGCGAGATCGTTCA[C/T]GCCTGTCCCTATGATGTCCCCTTTC
Phenotype
MIM: 613384
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CCNL1 PubMed Links

Gene Details

Gene
CCNL1
Gene Name
cyclin L1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308185.1 1633 Intron NP_001295114.1
NM_020307.3 1633 Missense Mutation CAT,CGT H499R NP_064703.1
XM_005247648.3 1633 Missense Mutation CAT,CGT H344R XP_005247705.1
XM_006713710.3 1633 Missense Mutation CAT,CGT H466R XP_006713773.1
XM_011513011.2 1633 Missense Mutation CAT,CGT H344R XP_011511313.1
XM_017006891.1 1633 Missense Mutation CAT,CGT H293R XP_016862380.1
XM_017006892.1 1633 Missense Mutation CAT,CGT H272R XP_016862381.1
XM_017006893.1 1633 Missense Mutation CAT,CGT H272R XP_016862382.1
XM_017006894.1 1633 Missense Mutation CAT,CGT H272R XP_016862383.1
XM_017006895.1 1633 Missense Mutation CAT,CGT H272R XP_016862384.1
XM_017006896.1 1633 Missense Mutation CAT,CGT H272R XP_016862385.1
XM_017006897.1 1633 Missense Mutation CAT,CGT H260R XP_016862386.1

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