Product Details

SNP ID

rs184771146

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:34111421 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGCATGACCCTGGCGTTGAAGCC[A/G]TGTCCTCCCAGGTAGCCGTTCCTGG

Phenotype

MIM: 606745

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PARD3 PubMed Links

Gene Details

Gene

PARD3

Gene Name

par-3 family cell polarity regulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001184785.1	3972	Silent Mutation	CAC,CAT	H1270H	NP_001171714.1
NM_001184786.1	3972	Silent Mutation	CAC,CAT	H1257H	NP_001171715.1
NM_001184787.1	3972	Silent Mutation	CAC,CAT	H1236H	NP_001171716.1
NM_001184788.1	3972	Silent Mutation	CAC,CAT	H1227H	NP_001171717.1
NM_001184789.1	3972	Silent Mutation	CAC,CAT	H1190H	NP_001171718.1
NM_001184790.1	3972	Silent Mutation	CAC,CAT	H1183H	NP_001171719.1
NM_001184791.1	3972	Silent Mutation	CAC,CAT	H1161H	NP_001171720.1
NM_001184792.1	3972	Intron			NP_001171721.1
NM_001184793.1	3972	Intron			NP_001171722.1
NM_001184794.1	3972	Intron			NP_001171723.1
NM_019619.3	3972	Silent Mutation	CAC,CAT	H1273H	NP_062565.2
XM_005252528.4	3972	Silent Mutation	CAC,CAT	H1269H	XP_005252585.1
XM_005252530.4	3972	Silent Mutation	CAC,CAT	H1255H	XP_005252587.1
XM_005252531.4	3972	Silent Mutation	CAC,CAT	H1240H	XP_005252588.1
XM_005252532.4	3972	Silent Mutation	CAC,CAT	H1226H	XP_005252589.1
XM_005252534.4	3972	Intron			XP_005252591.1
XM_005252535.4	3972	Intron			XP_005252592.1
XM_005252536.4	3972	Intron			XP_005252593.1
XM_011519569.2	3972	Silent Mutation	CAC,CAT	H1272H	XP_011517871.1
XM_011519570.2	3972	Silent Mutation	CAC,CAT	H1260H	XP_011517872.1
XM_011519571.2	3972	Silent Mutation	CAC,CAT	H1258H	XP_011517873.1
XM_011519572.2	3972	Silent Mutation	CAC,CAT	H1257H	XP_011517874.1
XM_011519573.2	3972	Silent Mutation	CAC,CAT	H1243H	XP_011517875.1
XM_011519575.2	3972	Silent Mutation	CAC,CAT	H1239H	XP_011517877.1
XM_011519576.2	3972	Silent Mutation	CAC,CAT	H1229H	XP_011517878.1
XM_011519577.2	3972	Silent Mutation	CAC,CAT	H1217H	XP_011517879.1
XM_011519578.2	3972	Silent Mutation	CAC,CAT	H1215H	XP_011517880.1
XM_011519579.2	3972	Silent Mutation	CAC,CAT	H1195H	XP_011517881.1
XM_011519581.2	3972	Intron			XP_011517883.1
XM_011519583.2	3972	Intron			XP_011517885.1
XM_011519584.2	3972	Intron			XP_011517886.1
XM_017016430.1	3972	Intron			XP_016871919.1

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