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TGGGGCTCAAGTATCTCCCGATCAT[C/G]TGGGACTCCGGGTTGCAGCTCCGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 609644 MIM: 186947 | ||||||||||||||||||||
Literature Links: |
FANCM 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 |
FANCM - Fanconi anemia complementation group M | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308133.1 | 151 | Missense Mutation | TCT,TGT | S,C 20 | NP_001295062.1 | |
NM_001308134.1 | 151 | Missense Mutation | TCT,TGT | S,C 20 | NP_001295063.1 | |
NM_020937.3 | 151 | Missense Mutation | TCT,TGT | S,C 20 | NP_065988.1 | |
XM_011537034.2 | 151 | Missense Mutation | TCT,TGT | S,C 20 | XP_011535336.1 | |
XM_011537035.2 | 151 | Missense Mutation | TCT,TGT | S,C 20 | XP_011535337.1 | |
XM_011537037.2 | 151 | Intron | XP_011535339.1 | |||
XM_017021523.1 | 151 | Missense Mutation | TCT,TGT | S,C 20 | XP_016877012.1 | |
XM_017021524.1 | 151 | Intron | XP_016877013.1 | |||
XM_017021525.1 | 151 | UTR 5 | XP_016877014.1 | |||
XM_017021526.1 | 151 | Intron | XP_016877015.1 | |||
XM_017021527.1 | 151 | UTR 5 | XP_016877016.1 |
FKBP3 - FK506 binding protein 3 | ||||||
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There are no transcripts associated with this gene. |