Product Details

SNP ID

rs2137895

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:53458824 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTAATAAAATAGTGAACCAATAGT[A/T]TGTGAGAGATTTTGACTTACTACAT

Phenotype

MIM: 607686 MIM: 609732

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FIP1L1 PubMed Links

Gene Details

Gene

FIP1L1

Gene Name

factor interacting with PAPOLA and CPSF1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134937.1	4774	Intron			NP_001128409.1
NM_001134938.1	4774	Intron			NP_001128410.1
NM_030917.3	4774	Intron			NP_112179.2
XM_005265769.4	4774	Intron			XP_005265826.1
XM_005265773.4	4774	Intron			XP_005265830.1
XM_005265774.4	4774	Intron			XP_005265831.1
XM_005265778.4	4774	Intron			XP_005265835.1
XM_005265779.4	4774	Intron			XP_005265836.1
XM_005265781.4	4774	Intron			XP_005265838.1
XM_005265782.4	4774	Intron			XP_005265839.1
XM_017008662.1	4774	Intron			XP_016864151.1
XM_017008663.1	4774	Intron			XP_016864152.1
XM_017008664.1	4774	Intron			XP_016864153.1
XM_017008665.1	4774	Intron			XP_016864154.1
XM_017008666.1	4774	Intron			XP_016864155.1
XM_017008667.1	4774	Intron			XP_016864156.1
XM_017008668.1	4774	Intron			XP_016864157.1
XM_017008669.1	4774	Intron			XP_016864158.1
XM_017008670.1	4774	Intron			XP_016864159.1
XM_017008671.1	4774	Intron			XP_016864160.1

Gene

LNX1

Gene Name

ligand of numb-protein X 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001126328.2	4774	Intron			NP_001119800.1
NM_032622.2	4774	Intron			NP_116011.2
XM_005265785.4	4774	UTR 3			XP_005265842.1
XM_017008776.1	4774	UTR 3			XP_016864265.1

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