Product Details

SNP ID

rs80289104

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:88572080 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACCAACATCTTTGATAGTAACGTG[C/G]CTTCAAACAAGAGCAATTTCAGTCG

Phenotype

MIM: 613279

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

ZC3H14 PubMed Links

Gene Details

Gene

ZC3H14

Gene Name

zinc finger CCCH-type containing 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001160103.1	506	Missense Mutation	CCT,GCT	P96A	NP_001153575.1
NM_001160104.1	506	Missense Mutation	CCT,GCT	P96A	NP_001153576.1
NM_001326295.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313224.1
NM_001326296.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313225.1
NM_001326297.1	506	Missense Mutation	CCT,GCT	P62A	NP_001313226.1
NM_001326298.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313227.1
NM_001326299.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313228.1
NM_001326300.1	506	UTR 5			NP_001313229.1
NM_001326301.1	506	Missense Mutation	CCT,GCT	P62A	NP_001313230.1
NM_001326302.1	506	UTR 5			NP_001313231.1
NM_001326303.1	506	Missense Mutation	CCT,GCT	P62A	NP_001313232.1
NM_001326304.1	506	UTR 5			NP_001313233.1
NM_001326305.1	506	UTR 5			NP_001313234.1
NM_001326306.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313235.1
NM_001326307.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313236.1
NM_001326308.1	506	UTR 5			NP_001313237.1
NM_001326309.1	506	UTR 5			NP_001313238.1
NM_001326310.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313239.1
NM_001326311.1	506	UTR 5			NP_001313240.1
NM_001326312.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313241.1
NM_001326313.1	506	Missense Mutation	CCT,GCT	P96A	NP_001313242.1
NM_001326314.1	506	UTR 5			NP_001313243.1
NM_001326315.1	506	Missense Mutation	CCT,GCT	P62A	NP_001313244.1
NM_001326316.1	506	Missense Mutation	CCT,GCT	P62A	NP_001313245.1
NM_024824.4	506	Missense Mutation	CCT,GCT	P96A	NP_079100.2
NM_207660.3	506	Missense Mutation	CCT,GCT	P96A	NP_997543.1
NM_207661.2	506	Missense Mutation	CCT,GCT	P62A	NP_997544.1
NM_207662.3	506	Intron			NP_997545.2
XM_005268067.4	506	Missense Mutation	CCT,GCT	P96A	XP_005268124.1
XM_005268068.4	506	Missense Mutation	CCT,GCT	P96A	XP_005268125.1
XM_005268069.4	506	Missense Mutation	CCT,GCT	P96A	XP_005268126.1
XM_005268070.4	506	Missense Mutation	CCT,GCT	P96A	XP_005268127.1
XM_005268071.4	506	Missense Mutation	CCT,GCT	P96A	XP_005268128.1
XM_005268073.3	506	Intron			XP_005268130.1
XM_006720257.2	506	Intron			XP_006720320.1
XM_011537160.2	506	Missense Mutation	CCT,GCT	P62A	XP_011535462.1
XM_011537161.2	506	Missense Mutation	CCT,GCT	P96A	XP_011535463.1
XM_011537162.2	506	Missense Mutation	CCT,GCT	P96A	XP_011535464.1
XM_017021648.1	506	Missense Mutation	CCT,GCT	P96A	XP_016877137.1
XM_017021649.1	506	Missense Mutation	CCT,GCT	P96A	XP_016877138.1
XM_017021650.1	506	Missense Mutation	CCT,GCT	P96A	XP_016877139.1

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