Product Details

SNP ID

rs148080961

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:70958286 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAATACTGCTGCGTGGAATGAATC[A/G]GCATTGTTCCTAGAGTTTGTCTCTC

Phenotype

MIM: 605515

Polymorphism

A/G, Transition 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	3363	Intron			NP_001012523.1
NM_001244808.1	3363	UTR 3			NP_001231737.1
NM_001244810.1	3363	UTR 3			NP_001231739.1
NM_001244812.1	3363	UTR 3			NP_001231741.1
NM_001244813.1	3363	UTR 3			NP_001231742.1
NM_001244814.1	3363	UTR 3			NP_001231743.1
NM_001244815.1	3363	UTR 3			NP_001231744.1
NM_001244816.1	3363	UTR 3			NP_001231745.1
NM_032682.5	3363	UTR 3			NP_116071.2
XM_005264735.3	3363	Intron			XP_005264792.1
XM_005264736.3	3363	Intron			XP_005264793.1
XM_005264737.4	3363	Intron			XP_005264794.1
XM_005264742.3	3363	Intron			XP_005264799.1
XM_006713102.2	3363	UTR 3			XP_006713165.1
XM_006713103.2	3363	Intron			XP_006713166.1
XM_006713104.2	3363	Intron			XP_006713167.1
XM_011533584.2	3363	UTR 3			XP_011531886.1
XM_011533585.2	3363	UTR 3			XP_011531887.1
XM_011533588.2	3363	Intron			XP_011531890.1
XM_017006165.1	3363	UTR 3			XP_016861654.1
XM_017006166.1	3363	Intron			XP_016861655.1
XM_017006167.1	3363	Intron			XP_016861656.1
XM_017006168.1	3363	Intron			XP_016861657.1

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