Product Details

SNP ID

rs117059294

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:22455292 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATTCTGATGACACAGTAGCTACA[A/G]AGGATTAATTTTAAAAATATTAATT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C2CD5 PubMed Links

Gene Details

Gene

C2CD5

Gene Name

C2 calcium dependent domain containing 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286173.1		Intron			NP_001273102.1
NM_001286174.1		Intron			NP_001273103.1
NM_001286175.1		Intron			NP_001273104.1
NM_001286176.1		Intron			NP_001273105.1
NM_001286177.1		Intron			NP_001273106.1
NM_014802.2		Intron			NP_055617.1
XM_005253538.2		Intron			XP_005253595.1
XM_005253539.3		Intron			XP_005253596.1
XM_006719170.2		Intron			XP_006719233.1
XM_017020264.1		Intron			XP_016875753.1
XM_017020265.1		Intron			XP_016875754.1
XM_017020266.1		Intron			XP_016875755.1
XM_017020267.1		Intron			XP_016875756.1
XM_017020268.1		Intron			XP_016875757.1
XM_017020269.1		Intron			XP_016875758.1
XM_017020270.1		Intron			XP_016875759.1
XM_017020271.1		Intron			XP_016875760.1
XM_017020272.1		Intron			XP_016875761.1
XM_017020273.1		Intron			XP_016875762.1
XM_017020274.1		Intron			XP_016875763.1
XM_017020275.1		Intron			XP_016875764.1
XM_017020276.1		Intron			XP_016875765.1
XM_017020277.1		Intron			XP_016875766.1
XM_017020278.1		Intron			XP_016875767.1
XM_017020279.1		Intron			XP_016875768.1

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