Product Details

SNP ID

rs148086727

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:113954250 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCGGGCAGTCTCAACAATCGCACA[A/G]CAAAGGATGACCCCAAGGGCTCTTC

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CCDC191 PubMed Links

Additional Information

For this assay, SNP(s) [rs11921691] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CCDC191

Gene Name

coiled-coil domain containing 191

There are no transcripts associated with this gene.

Gene

GRAMD1C

Gene Name

GRAM domain containing 1C

There are no transcripts associated with this gene.

Gene

ZDHHC23

Gene Name

zinc finger DHHC-type containing 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320466.1	934	Missense Mutation	ACA,GCA	T238A	NP_001307395.1
NM_001320467.1	934	Missense Mutation	ACA,GCA	T238A	NP_001307396.1
NM_001320468.1	934	Missense Mutation	ACA,GCA	T238A	NP_001307397.1
NM_173570.4	934	Missense Mutation	ACA,GCA	T238A	NP_775841.2
XM_005247269.1	934	Missense Mutation	ACA,GCA	T238A	XP_005247326.1
XM_005247270.3	934	Missense Mutation	ACA,GCA	T77A	XP_005247327.1
XM_006713562.3	934	Missense Mutation	ACA,GCA	T238A	XP_006713625.1
XM_011512618.2	934	Missense Mutation	ACA,GCA	T238A	XP_011510920.1
XM_011512619.1	934	Missense Mutation	ACA,GCA	T238A	XP_011510921.1
XM_017006084.1	934	Missense Mutation	ACA,GCA	T238A	XP_016861573.1
XM_017006085.1	934	Missense Mutation	ACA,GCA	T238A	XP_016861574.1
XM_017006086.1	934	Missense Mutation	ACA,GCA	T238A	XP_016861575.1
XM_017006087.1	934	Missense Mutation	ACA,GCA	T238A	XP_016861576.1

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