Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACAGTCATTCATGTTTTAACACTGC[C/T]GTTTATGTGTGGATACTGAGGAAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176943 | ||||||||||||||||||||
Literature Links: |
FGFR2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FGFR2 - fibroblast growth factor receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000141.4 | 3383 | Missense Mutation | AGC,GGC | S,G 817 | NP_000132.3 | |
NM_001144913.1 | 3383 | Intron | NP_001138385.1 | |||
NM_001144914.1 | 3383 | Missense Mutation | AGC,GGC | S,G 705 | NP_001138386.1 | |
NM_001144915.1 | 3383 | Intron | NP_001138387.1 | |||
NM_001144916.1 | 3383 | Missense Mutation | AGC,GGC | S,G 702 | NP_001138388.1 | |
NM_001144917.1 | 3383 | Missense Mutation | AGC,GGC | S,G 701 | NP_001138389.1 | |
NM_001144918.1 | 3383 | Missense Mutation | AGC,GGC | S,G 700 | NP_001138390.1 | |
NM_001144919.1 | 3383 | Intron | NP_001138391.1 | |||
NM_001320654.1 | 3383 | Missense Mutation | AGC,GGC | S,G 589 | NP_001307583.1 | |
NM_001320658.1 | 3383 | Missense Mutation | AGC,GGC | S,G 815 | NP_001307587.1 | |
NM_022970.3 | 3383 | Missense Mutation | AGC,GGC | S,G 818 | NP_075259.4 | |
NM_023029.2 | 3383 | Missense Mutation | AGC,GGC | S,G 728 | NP_075418.1 | |
XM_006717708.2 | 3383 | Missense Mutation | AGC,GGC | S,G 835 | XP_006717771.1 | |
XM_006717710.3 | 3383 | UTR 3 | XP_006717773.1 | |||
XM_006717711.2 | 3383 | Missense Mutation | AGC,GGC | S,G 748 | XP_006717774.1 | |
XM_006717712.2 | 3383 | Missense Mutation | AGC,GGC | S,G 722 | XP_006717775.1 | |
XM_017015920.1 | 3383 | UTR 3 | XP_016871409.1 | |||
XM_017015921.1 | 3383 | UTR 3 | XP_016871410.1 | |||
XM_017015922.1 | 3383 | Missense Mutation | AGC,GGC | S,G 746 | XP_016871411.1 | |
XM_017015923.1 | 3383 | Missense Mutation | AGC,GGC | S,G 745 | XP_016871412.1 | |
XM_017015924.1 | 3383 | Missense Mutation | AGC,GGC | S,G 721 | XP_016871413.1 | |
XM_017015925.1 | 3383 | UTR 3 | XP_016871414.1 |