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SNP ID: rs150977299
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:56813776 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGTACTTCTCATCAGCTTGATTGG[C/T]ACCACCTGTGCTGGTGCTGGCACGT
Phenotype: MIM: 601483
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: PEG3 PubMed Links

Gene Details

Gene: PEG3
Gene Name: paternally expressed 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146184.1	4670	Missense Mutation	ACC,GCC	T1556A	NP_001139656.1
NM_001146185.1	4670	Missense Mutation	ACC,GCC	T1430A	NP_001139657.1
NM_001146186.1	4670	Missense Mutation	ACC,GCC	T1556A	NP_001139658.1
NM_001146187.1	4670	Missense Mutation	ACC,GCC	T1432A	NP_001139659.1
NM_006210.2	4670	Missense Mutation	ACC,GCC	T1556A	NP_006201.1

Gene: PEG3-AS1
Gene Name: PEG3 antisense RNA 1

There are no transcripts associated with this gene.

Gene: ZIM2
Gene Name: zinc finger imprinted 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146326.1	4670	Intron			NP_001139798.1
NM_001146327.1	4670	Intron			NP_001139799.1
NM_015363.4	4670	Intron			NP_056178.3

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