Product Details

SNP ID

rs113891864

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:70959385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGGGGCTCTTCTTTGACGTGTAC[A/T]GGATGCCTGGAAAAAATATGCAGAG

Phenotype

MIM: 605515

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FOXP1 PubMed Links

Gene Details

Gene

FOXP1

Gene Name

forkhead box P1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012505.1	2360	Intron			NP_001012523.1
NM_001244808.1	2360	Silent Mutation	CCA,CCT	P631P	NP_001231737.1
NM_001244810.1	2360	Silent Mutation	CCA,CCT	P648P	NP_001231739.1
NM_001244812.1	2360	Silent Mutation	CCA,CCT	P556P	NP_001231741.1
NM_001244813.1	2360	Silent Mutation	CCA,CCT	P532P	NP_001231742.1
NM_001244814.1	2360	Silent Mutation	CCA,CCT	P632P	NP_001231743.1
NM_001244815.1	2360	Silent Mutation	CCA,CCT	P634P	NP_001231744.1
NM_001244816.1	2360	Silent Mutation	CCA,CCT	P632P	NP_001231745.1
NM_032682.5	2360	Silent Mutation	CCA,CCT	P632P	NP_116071.2
XM_005264735.3	2360	Silent Mutation	CCA,CCT	P633P	XP_005264792.1
XM_005264736.3	2360	Silent Mutation	CCA,CCT	P633P	XP_005264793.1
XM_005264737.4	2360	Silent Mutation	CCA,CCT	P631P	XP_005264794.1
XM_005264742.3	2360	Silent Mutation	CCA,CCT	P531P	XP_005264799.1
XM_006713102.2	2360	Silent Mutation	CCA,CCT	P632P	XP_006713165.1
XM_006713103.2	2360	Silent Mutation	CCA,CCT	P632P	XP_006713166.1
XM_006713104.2	2360	Silent Mutation	CCA,CCT	P632P	XP_006713167.1
XM_011533584.2	2360	Silent Mutation	CCA,CCT	P632P	XP_011531886.1
XM_011533585.2	2360	Silent Mutation	CCA,CCT	P632P	XP_011531887.1
XM_011533588.2	2360	Silent Mutation	CCA,CCT	P532P	XP_011531890.1
XM_017006165.1	2360	Silent Mutation	CCA,CCT	P632P	XP_016861654.1
XM_017006166.1	2360	Silent Mutation	CCA,CCT	P632P	XP_016861655.1
XM_017006167.1	2360	Silent Mutation	CCA,CCT	P632P	XP_016861656.1
XM_017006168.1	2360	Intron			XP_016861657.1

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