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CCAGCATCAGGATCACCAGGCTGGT[A/G]TTGAGGCAGCTGACGTTCTCCTGCA
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
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
MYH7B - myosin heavy chain 7B | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
TRPC4AP - transient receptor potential cation channel subfamily C member 4 associated protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015638.2 | 1582 | Silent Mutation | NP_056453.1 | |||
NM_199368.1 | 1582 | Silent Mutation | NP_955400.1 | |||
XM_011528772.2 | 1582 | Intron | XP_011527074.1 | |||
XM_011528774.1 | 1582 | Silent Mutation | XP_011527076.1 | |||
XM_017027799.1 | 1582 | Intron | XP_016883288.1 | |||
XM_017027800.1 | 1582 | Silent Mutation | XP_016883289.1 | |||
XM_017027801.1 | 1582 | Silent Mutation | XP_016883290.1 |