Product Details

SNP ID

rs141746561

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:53462822 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTATGAATTTCATTAAATTTCCTA[C/T]TGTAAAATATTTATCTGCTGCATTT

Phenotype

MIM: 607686 MIM: 609732

Polymorphism

C/T, Transition 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		Intron			NP_001128409.1
NM_001134938.1		Intron			NP_001128410.1
NM_030917.3		Intron			NP_112179.2
XM_005265769.4		Intron			XP_005265826.1
XM_005265773.4		Intron			XP_005265830.1
XM_005265774.4		Intron			XP_005265831.1
XM_005265778.4		Intron			XP_005265835.1
XM_005265779.4		Intron			XP_005265836.1
XM_005265781.4		Intron			XP_005265838.1
XM_005265782.4		Intron			XP_005265839.1
XM_017008662.1		Intron			XP_016864151.1
XM_017008663.1		Intron			XP_016864152.1
XM_017008664.1		Intron			XP_016864153.1
XM_017008665.1		Intron			XP_016864154.1
XM_017008666.1		Intron			XP_016864155.1
XM_017008667.1		Intron			XP_016864156.1
XM_017008668.1		Intron			XP_016864157.1
XM_017008669.1		Intron			XP_016864158.1
XM_017008670.1		Intron			XP_016864159.1
XM_017008671.1		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		Intron			NP_001119800.1
NM_032622.2		Intron			NP_116011.2
XM_005265785.4		Intron			XP_005265842.1
XM_017008776.1		Intron			XP_016864265.1

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