Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCAGAGGGTGACTGCCGGTCCGGG[C/T]TCAACAGGATGGACACTGTCTCCTT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MYH7B - myosin heavy chain 7B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020884.4 | 1821 | Intron | NP_065935.3 | |||
XM_006723840.3 | 1821 | Intron | XP_006723903.1 | |||
XM_011528941.2 | 1821 | Intron | XP_011527243.1 | |||
XM_011528947.2 | 1821 | Intron | XP_011527249.1 | |||
XM_011528948.2 | 1821 | Intron | XP_011527250.1 | |||
XM_017027986.1 | 1821 | Intron | XP_016883475.1 | |||
XM_017027987.1 | 1821 | Intron | XP_016883476.1 |
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 | 1821 | Missense Mutation | AAC,AGC | N,S 770 | NP_056453.1 | |
NM_199368.1 | 1821 | Missense Mutation | AAC,AGC | N,S 762 | NP_955400.1 | |
XM_011528772.2 | 1821 | Intron | XP_011527074.1 | |||
XM_011528774.1 | 1821 | Missense Mutation | AAC,AGC | N,S 372 | XP_011527076.1 | |
XM_017027799.1 | 1821 | Intron | XP_016883288.1 | |||
XM_017027800.1 | 1821 | Missense Mutation | AAC,AGC | N,S 432 | XP_016883289.1 | |
XM_017027801.1 | 1821 | Missense Mutation | AAC,AGC | N,S 372 | XP_016883290.1 |