Product Details

SNP ID

rs199703562

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:157150166 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACCAATGGGGACGAGTTGGCAACG[C/G]AATCTAAACCATAAGAACAGAATGT

Phenotype

MIM: 613384

Polymorphism

C/G, Transversion 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	915	Missense Mutation	CCG,GCG	P260A	NP_001295114.1
NM_020307.3	915	Missense Mutation	CCG,GCG	P260A	NP_064703.1
XM_005247648.3	915	Missense Mutation	CCG,GCG	P105A	XP_005247705.1
XM_006713710.3	915	Missense Mutation	CCG,GCG	P260A	XP_006713773.1
XM_011513011.2	915	Missense Mutation	CCG,GCG	P105A	XP_011511313.1
XM_017006891.1	915	Missense Mutation	CCG,GCG	P54A	XP_016862380.1
XM_017006892.1	915	Missense Mutation	CCG,GCG	P33A	XP_016862381.1
XM_017006893.1	915	Missense Mutation	CCG,GCG	P33A	XP_016862382.1
XM_017006894.1	915	Missense Mutation	CCG,GCG	P33A	XP_016862383.1
XM_017006895.1	915	Missense Mutation	CCG,GCG	P33A	XP_016862384.1
XM_017006896.1	915	Missense Mutation	CCG,GCG	P33A	XP_016862385.1
XM_017006897.1	915	Missense Mutation	CCG,GCG	P54A	XP_016862386.1

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