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TGTCCTCCGCCCGCCGCCGCCTCAC[C/T]GGTGAGCTTCCTGAGCCGTCGCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614144 MIM: 602521 MIM: 600596 | ||||||||||||||||||||
Literature Links: |
B9D1 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 |
B9D1 - B9 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243473.2 | 617 | Intron | NP_001230402.1 | |||
NM_001243475.2 | 617 | Intron | NP_001230404.1 | |||
NM_001321214.1 | 617 | Intron | NP_001308143.1 | |||
NM_001321215.1 | 617 | Intron | NP_001308144.1 | |||
NM_001321216.1 | 617 | Intron | NP_001308145.1 | |||
NM_001321217.1 | 617 | Intron | NP_001308146.1 | |||
NM_001321218.1 | 617 | Intron | NP_001308147.1 | |||
NM_001321219.1 | 617 | Intron | NP_001308148.1 | |||
NM_015681.4 | 617 | Intron | NP_056496.1 | |||
XM_005256607.2 | 617 | Intron | XP_005256664.1 | |||
XM_005256610.1 | 617 | Intron | XP_005256667.1 | |||
XM_017024452.1 | 617 | Intron | XP_016879941.1 |
MAPK7 - mitogen-activated protein kinase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002749.3 | 617 | Silent Mutation | ACC,ACT | T,T 77 | NP_002740.2 | |
NM_139032.2 | 617 | Intron | NP_620601.1 | |||
NM_139033.2 | 617 | Silent Mutation | ACC,ACT | T,T 77 | NP_620602.2 | |
NM_139034.2 | 617 | Silent Mutation | ACC,ACT | T,T 77 | NP_620603.2 | |
XM_006721557.3 | 617 | Silent Mutation | ACC,ACT | T,T 77 | XP_006721620.1 | |
XM_006721558.3 | 617 | Silent Mutation | ACC,ACT | T,T 77 | XP_006721621.1 | |
XM_006721559.3 | 617 | Silent Mutation | ACC,ACT | T,T 77 | XP_006721622.1 | |
XM_011523957.2 | 617 | Intron | XP_011522259.1 |
MFAP4 - microfibrillar associated protein 4 | ||||||
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There are no transcripts associated with this gene. |