Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATTATTCTTTTCCATTTCAGTAAAA[G/T]ATAATGTGCATGGCTCTGGGAACAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 134580 | ||||||||||||||||||||
Literature Links: |
F13B 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 |
F13B - coagulation factor XIII B chain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001994.2 | 1792 | Missense Mutation | NP_001985.2 | |||
XM_011509283.2 | 1792 | Missense Mutation | XP_011507585.1 | |||
XM_011509284.2 | 1792 | Missense Mutation | XP_011507586.1 | |||
XM_011509286.2 | 1792 | Missense Mutation | XP_011507588.1 |