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GGGGTACTTCTTGCTGTGCTCCATC[C/T]GCTGCAGCAGCCGCAGGTACAGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609928 MIM: 608430 | ||||||||||||||||||||
Literature Links: |
MYH7B 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 |
MYH7B - myosin heavy chain 7B | ||||||
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There are no transcripts associated with this gene. |
TRPC4AP - transient receptor potential cation channel subfamily C member 4 associated protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015638.2 | 1653 | Missense Mutation | CAG,CGG | Q,R 714 | NP_056453.1 | |
NM_199368.1 | 1653 | Missense Mutation | CAG,CGG | Q,R 706 | NP_955400.1 | |
XM_011528772.2 | 1653 | Intron | XP_011527074.1 | |||
XM_011528774.1 | 1653 | Missense Mutation | CAG,CGG | Q,R 316 | XP_011527076.1 | |
XM_017027799.1 | 1653 | Intron | XP_016883288.1 | |||
XM_017027800.1 | 1653 | Missense Mutation | CAG,CGG | Q,R 376 | XP_016883289.1 | |
XM_017027801.1 | 1653 | Missense Mutation | CAG,CGG | Q,R 316 | XP_016883290.1 |