Product Details

SNP ID

rs142282210

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:134964859 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGTCTTGATGTATATTCAGTGACT[A/T]CTCTCCAAGAAGGAGTGCTTCAGGA

Phenotype

MIM: 603862

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

CCNT2 PubMed Links

Gene Details

Gene

CCNT2

Gene Name

cyclin T2

There are no transcripts associated with this gene.

Gene

MAP3K19

Gene Name

mitogen-activated protein kinase kinase kinase 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018044.2	3670	Missense Mutation	AGA,AGT	R1213S	NP_001018054.1
NM_001018046.2	3670	Missense Mutation	AGA,AGT	R508S	NP_001018056.1
NM_001018047.2	3670	Missense Mutation	AGA,AGT	R460S	NP_001018057.1
NM_001282883.1	3670	Missense Mutation	AGA,AGT	R458S	NP_001269812.1
NM_001321177.1	3670	Intron			NP_001308106.1
NM_025052.4	3670	Missense Mutation	AGA,AGT	R1326S	NP_079328.3
XM_011511891.2	3670	Missense Mutation	AGA,AGT	R1343S	XP_011510193.1
XM_011511892.1	3670	Missense Mutation	AGA,AGT	R1326S	XP_011510194.1
XM_011511894.2	3670	Missense Mutation	AGA,AGT	R1298S	XP_011510196.1
XM_011511896.2	3670	Missense Mutation	AGA,AGT	R1231S	XP_011510198.1
XM_011511897.2	3670	Missense Mutation	AGA,AGT	R1231S	XP_011510199.1
XM_017005003.1	3670	Missense Mutation	AGA,AGT	R1326S	XP_016860492.1
XM_017005004.1	3670	Missense Mutation	AGA,AGT	R1298S	XP_016860493.1
XM_017005005.1	3670	Missense Mutation	AGA,AGT	R1298S	XP_016860494.1
XM_017005006.1	3670	Missense Mutation	AGA,AGT	R1204S	XP_016860495.1
XM_017005007.1	3670	Intron			XP_016860496.1

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