Product Details

SNP ID

rs200191417

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:157149546 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGGTTCTTTTTTGACTGTCTTCA[C/T]ATTAATGGAGATTGGTGATTTCTCT

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	1209	Missense Mutation	ATG,GTG	M358V	NP_001295114.1
NM_020307.3	1209	Missense Mutation	ATG,GTG	M358V	NP_064703.1
XM_005247648.3	1209	Missense Mutation	ATG,GTG	M203V	XP_005247705.1
XM_006713710.3	1209	Missense Mutation	ATG,GTG	M358V	XP_006713773.1
XM_011513011.2	1209	Missense Mutation	ATG,GTG	M203V	XP_011511313.1
XM_017006891.1	1209	Missense Mutation	ATG,GTG	M152V	XP_016862380.1
XM_017006892.1	1209	Missense Mutation	ATG,GTG	M131V	XP_016862381.1
XM_017006893.1	1209	Missense Mutation	ATG,GTG	M131V	XP_016862382.1
XM_017006894.1	1209	Missense Mutation	ATG,GTG	M131V	XP_016862383.1
XM_017006895.1	1209	Missense Mutation	ATG,GTG	M131V	XP_016862384.1
XM_017006896.1	1209	Missense Mutation	ATG,GTG	M131V	XP_016862385.1
XM_017006897.1	1209	Missense Mutation	ATG,GTG	M152V	XP_016862386.1

View Full Product Details