Product Details

SNP ID

rs3814880

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:30006574 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGCCCCTCCCTGGCCTCCCTCCA[T/C]GTCCCGTCCCCTCCTGGGTACCTCG

Phenotype

MIM: 604567

Polymorphism

T/C, Transition substitution

Allele Nomenclature

Literature Links

DOC2A PubMed Links

Gene Details

Gene

DOC2A

Gene Name

double C2 domain alpha

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282062.1		Intron			NP_001268991.1
NM_001282063.1		Intron			NP_001268992.1
NM_001282068.1		Intron			NP_001268997.1
NM_003586.2		Intron			NP_003577.2
XM_011545975.1		Intron			XP_011544277.1
XM_017023776.1		Intron			XP_016879265.1
XM_017023777.1		Intron			XP_016879266.1
XM_017023778.1		Intron			XP_016879267.1

Gene

INO80E

Gene Name

INO80 complex subunit E

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304562.1		Intron			NP_001291491.1
NM_001304563.1		Intron			NP_001291492.1
NM_173618.2		Intron			NP_775889.1
XM_011545809.2		Intron			XP_011544111.1
XM_011545811.2		Intron			XP_011544113.1
XM_011545812.2		Intron			XP_011544114.1
XM_017023169.1		Intron			XP_016878658.1

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