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Search Thermo Fisher Scientific
TATCTCAGAACCTGTCCCTCAAGCC[A/G]GCTAATCTGTAAGTATGAGAACATA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614043 MIM: 120436 | |||||||||||||||||||||||
Literature Links: |
LRRFIP2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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 |
LRRFIP2 - LRR binding FLII interacting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134369.2 | 1753 | Missense Mutation | CGG,TGG | R,W 356 | NP_001127841.1 | |
NM_001282691.1 | 1753 | Missense Mutation | CGG,TGG | R,W 435 | NP_001269620.1 | |
NM_006309.3 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | NP_006300.1 | |
NM_017724.2 | 1753 | Missense Mutation | CGG,TGG | R,W 332 | NP_060194.1 | |
XM_005265539.2 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | XP_005265596.1 | |
XM_005265540.1 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | XP_005265597.1 | |
XM_005265550.1 | 1753 | Missense Mutation | CGG,TGG | R,W 509 | XP_005265607.1 | |
XM_005265551.1 | 1753 | Missense Mutation | CGG,TGG | R,W 472 | XP_005265608.1 | |
XM_005265553.1 | 1753 | Missense Mutation | CGG,TGG | R,W 421 | XP_005265610.1 | |
XM_005265554.2 | 1753 | Missense Mutation | CGG,TGG | R,W 421 | XP_005265611.1 | |
XM_005265556.1 | 1753 | Missense Mutation | CGG,TGG | R,W 397 | XP_005265613.1 | |
XM_006713385.1 | 1753 | Missense Mutation | CGG,TGG | R,W 652 | XP_006713448.1 | |
XM_006713386.1 | 1753 | Missense Mutation | CGG,TGG | R,W 639 | XP_006713449.1 | |
XM_006713387.1 | 1753 | Missense Mutation | CGG,TGG | R,W 638 | XP_006713450.1 | |
XM_006713388.1 | 1753 | Missense Mutation | CGG,TGG | R,W 637 | XP_006713451.1 | |
XM_006713389.1 | 1753 | Missense Mutation | CGG,TGG | R,W 636 | XP_006713452.1 | |
XM_006713390.1 | 1753 | Missense Mutation | CGG,TGG | R,W 636 | XP_006713453.1 | |
XM_006713392.1 | 1753 | Missense Mutation | CGG,TGG | R,W 629 | XP_006713455.1 | |
XM_006713393.1 | 1753 | Missense Mutation | CGG,TGG | R,W 623 | XP_006713456.1 | |
XM_006713394.1 | 1753 | Missense Mutation | CGG,TGG | R,W 622 | XP_006713457.1 | |
XM_006713395.1 | 1753 | Missense Mutation | CGG,TGG | R,W 622 | XP_006713458.1 | |
XM_006713396.1 | 1753 | Missense Mutation | CGG,TGG | R,W 617 | XP_006713459.1 | |
XM_006713397.1 | 1753 | Missense Mutation | CGG,TGG | R,W 581 | XP_006713460.1 | |
XM_006713400.1 | 1753 | Missense Mutation | CGG,TGG | R,W 436 | XP_006713463.1 | |
XM_006713404.1 | 1753 | Missense Mutation | CGG,TGG | R,W 347 | XP_006713467.1 | |
XM_011534217.1 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | XP_011532519.1 | |
XM_011534218.1 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | XP_011532520.1 | |
XM_011534219.1 | 1753 | Missense Mutation | CGG,TGG | R,W 653 | XP_011532521.1 | |
XM_011534221.1 | 1753 | Missense Mutation | CGG,TGG | R,W 617 | XP_011532523.1 | |
XM_011534222.1 | 1753 | Missense Mutation | CGG,TGG | R,W 588 | XP_011532524.1 | |
XM_011534229.1 | 1753 | Missense Mutation | CGG,TGG | R,W 436 | XP_011532531.1 | |
XM_017007465.1 | 1753 | Missense Mutation | CGG,TGG | R,W 602 | XP_016862954.1 | |
XM_017007466.1 | 1753 | Missense Mutation | CGG,TGG | R,W 600 | XP_016862955.1 | |
XM_017007467.1 | 1753 | Missense Mutation | CGG,TGG | R,W 598 | XP_016862956.1 | |
XM_017007468.1 | 1753 | Missense Mutation | CGG,TGG | R,W 566 | XP_016862957.1 | |
XM_017007469.1 | 1753 | Missense Mutation | CGG,TGG | R,W 564 | XP_016862958.1 | |
XM_017007470.1 | 1753 | Missense Mutation | CGG,TGG | R,W 552 | XP_016862959.1 | |
XM_017007471.1 | 1753 | Missense Mutation | CGG,TGG | R,W 455 | XP_016862960.1 | |
XM_017007472.1 | 1753 | Missense Mutation | CGG,TGG | R,W 441 | XP_016862961.1 | |
XM_017007473.1 | 1753 | Missense Mutation | CGG,TGG | R,W 431 | XP_016862962.1 | |
XM_017007474.1 | 1753 | Missense Mutation | CGG,TGG | R,W 424 | XP_016862963.1 | |
XM_017007475.1 | 1753 | Missense Mutation | CGG,TGG | R,W 424 | XP_016862964.1 | |
XM_017007476.1 | 1753 | Missense Mutation | CGG,TGG | R,W 421 | XP_016862965.1 | |
XM_017007477.1 | 1753 | Missense Mutation | CGG,TGG | R,W 400 | XP_016862966.1 | |
XM_017007478.1 | 1753 | Missense Mutation | CGG,TGG | R,W 390 | XP_016862967.1 | |
XM_017007479.1 | 1753 | Missense Mutation | CGG,TGG | R,W 390 | XP_016862968.1 | |
XM_017007480.1 | 1753 | Missense Mutation | CGG,TGG | R,W 390 | XP_016862969.1 | |
XM_017007481.1 | 1753 | Missense Mutation | CGG,TGG | R,W 387 | XP_016862970.1 | |
XM_017007482.1 | 1753 | Missense Mutation | CGG,TGG | R,W 366 | XP_016862971.1 | |
XM_017007483.1 | 1753 | Missense Mutation | CGG,TGG | R,W 356 | XP_016862972.1 | |
XM_017007484.1 | 1753 | Missense Mutation | CGG,TGG | R,W 356 | XP_016862973.1 |
MLH1 - mutL homolog 1 | ||||||
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There are no transcripts associated with this gene. |