Product Details

SNP ID

rs202044617

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:155659857 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACAATCCTTCTTGGCACTGTTTAT[C/T]GACTGGTGGAGGCCCTGGGCTATGT

Phenotype

MIM: 607860

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

YY1AP1 PubMed Links

Gene Details

Gene

YY1AP1

Gene Name

YY1 associated protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198899.1	2659	Missense Mutation	AAT,GAT	N674D	NP_001185828.1
NM_001198900.1	2659	Missense Mutation	AAT,GAT	N674D	NP_001185829.1
NM_001198901.1	2659	Missense Mutation	AAT,GAT	N685D	NP_001185830.1
NM_001198902.1	2659	Missense Mutation	AAT,GAT	N685D	NP_001185831.1
NM_001198903.1	2659	Missense Mutation	AAT,GAT	N823D	NP_001185832.1
NM_001198904.1	2659	Missense Mutation	AAT,GAT	N803D	NP_001185833.1
NM_001198905.1	2659	Missense Mutation	AAT,GAT	N665D	NP_001185834.1
NM_001198906.1	2659	UTR 3			NP_001185835.1
NM_018253.3	2659	Missense Mutation	AAT,GAT	N674D	NP_060723.2
NM_139118.2	2659	Missense Mutation	AAT,GAT	N731D	NP_620829.1
NM_139119.2	2659	Missense Mutation	AAT,GAT	N685D	NP_620830.1
NM_139121.2	2659	Missense Mutation	AAT,GAT	N619D	NP_620832.1

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