Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATTTCTGGGCTCTCACTGTTGGTG[A/G]CATCTAATCTGGATGGTTTAGATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604108 | ||||||||||||||||||||
Literature Links: |
MAP7 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 |
MAP7 - microtubule associated protein 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198608.1 | 3356 | Missense Mutation | GCC,GTC | A,V 731 | NP_001185537.1 | |
NM_001198609.1 | 3356 | Missense Mutation | GCC,GTC | A,V 739 | NP_001185538.1 | |
NM_001198611.1 | 3356 | Missense Mutation | GCC,GTC | A,V 694 | NP_001185540.1 | |
NM_001198614.1 | 3356 | Missense Mutation | GCC,GTC | A,V 731 | NP_001185543.1 | |
NM_001198615.1 | 3356 | Missense Mutation | GCC,GTC | A,V 694 | NP_001185544.1 | |
NM_001198616.1 | 3356 | Missense Mutation | GCC,GTC | A,V 672 | NP_001185545.1 | |
NM_001198617.1 | 3356 | Missense Mutation | GCC,GTC | A,V 615 | NP_001185546.1 | |
NM_001198618.1 | 3356 | Missense Mutation | GCC,GTC | A,V 563 | NP_001185547.1 | |
NM_001198619.1 | 3356 | Missense Mutation | GCC,GTC | A,V 563 | NP_001185548.1 | |
NM_003980.4 | 3356 | Missense Mutation | GCC,GTC | A,V 709 | NP_003971.1 | |
XM_006715598.2 | 3356 | Missense Mutation | GCC,GTC | A,V 739 | XP_006715661.1 | |
XM_006715599.2 | 3356 | Missense Mutation | GCC,GTC | A,V 739 | XP_006715662.1 | |
XM_006715600.2 | 3356 | Missense Mutation | GCC,GTC | A,V 731 | XP_006715663.1 | |
XM_006715601.3 | 3356 | Missense Mutation | GCC,GTC | A,V 717 | XP_006715664.1 | |
XM_011536243.2 | 3356 | Missense Mutation | GCC,GTC | A,V 702 | XP_011534545.1 | |
XM_011536244.2 | 3356 | Missense Mutation | GCC,GTC | A,V 702 | XP_011534546.1 | |
XM_011536245.1 | 3356 | Missense Mutation | GCC,GTC | A,V 680 | XP_011534547.1 | |
XM_011536246.2 | 3356 | Missense Mutation | GCC,GTC | A,V 665 | XP_011534548.1 | |
XM_017011471.1 | 3356 | Missense Mutation | GCC,GTC | A,V 694 | XP_016866960.1 |