Product Details

SNP ID

rs3135821

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:121481131 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGCAAAGCTGAAAATATTTACTC[C/T]CTGGCCCTTTACAGAAAGCAGTTGC

Phenotype

MIM: 176943

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FGFR2 PubMed Links

Additional Information

For this assay, SNP(s) [rs41294239] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

FGFR2

Gene Name

fibroblast growth factor receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000141.4		Intron			NP_000132.3
NM_001144913.1		Intron			NP_001138385.1
NM_001144914.1		Intron			NP_001138386.1
NM_001144915.1		Intron			NP_001138387.1
NM_001144916.1		Intron			NP_001138388.1
NM_001144917.1		Intron			NP_001138389.1
NM_001144918.1		Intron			NP_001138390.1
NM_001144919.1		Intron			NP_001138391.1
NM_001320654.1		Intron			NP_001307583.1
NM_001320658.1		Intron			NP_001307587.1
NM_022970.3		Intron			NP_075259.4
NM_023029.2		Intron			NP_075418.1
XM_006717708.2		Intron			XP_006717771.1
XM_006717710.3		Intron			XP_006717773.1
XM_006717711.2		Intron			XP_006717774.1
XM_006717712.2		Intron			XP_006717775.1
XM_017015920.1		Intron			XP_016871409.1
XM_017015921.1		Intron			XP_016871410.1
XM_017015922.1		Intron			XP_016871411.1
XM_017015923.1		Intron			XP_016871412.1
XM_017015924.1		Intron			XP_016871413.1
XM_017015925.1		Intron			XP_016871414.1

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