Product Details

SNP ID

rs140318221

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:121479866 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGCAGACACAGTCATTCATGTTTT[A/G]ACACTGCCGTTTATGTGTGGATACT

Phenotype

MIM: 176943

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FGFR2 PubMed Links

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	3391	Silent Mutation	GTC,GTT	V819V	NP_000132.3
NM_001144913.1	3391	Intron			NP_001138385.1
NM_001144914.1	3391	Silent Mutation	GTC,GTT	V707V	NP_001138386.1
NM_001144915.1	3391	Intron			NP_001138387.1
NM_001144916.1	3391	Silent Mutation	GTC,GTT	V704V	NP_001138388.1
NM_001144917.1	3391	Silent Mutation	GTC,GTT	V703V	NP_001138389.1
NM_001144918.1	3391	Silent Mutation	GTC,GTT	V702V	NP_001138390.1
NM_001144919.1	3391	Intron			NP_001138391.1
NM_001320654.1	3391	Silent Mutation	GTC,GTT	V591V	NP_001307583.1
NM_001320658.1	3391	Silent Mutation	GTC,GTT	V817V	NP_001307587.1
NM_022970.3	3391	Silent Mutation	GTC,GTT	V820V	NP_075259.4
NM_023029.2	3391	Silent Mutation	GTC,GTT	V730V	NP_075418.1
XM_006717708.2	3391	Silent Mutation	GTC,GTT	V837V	XP_006717771.1
XM_006717710.3	3391	UTR 3			XP_006717773.1
XM_006717711.2	3391	Silent Mutation	GTC,GTT	V750V	XP_006717774.1
XM_006717712.2	3391	Silent Mutation	GTC,GTT	V724V	XP_006717775.1
XM_017015920.1	3391	UTR 3			XP_016871409.1
XM_017015921.1	3391	UTR 3			XP_016871410.1
XM_017015922.1	3391	Silent Mutation	GTC,GTT	V748V	XP_016871411.1
XM_017015923.1	3391	Silent Mutation	GTC,GTT	V747V	XP_016871412.1
XM_017015924.1	3391	Silent Mutation	GTC,GTT	V723V	XP_016871413.1
XM_017015925.1	3391	UTR 3			XP_016871414.1

View Full Product Details