Product Details
- SNP ID
-
rs188430992
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:136345919 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGGGGCCCAAGTGTCCCTTCATCAT[C/T]AAAGGCCAAAATTGGATTCAAAGGA
- Phenotype
-
MIM: 604108
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MAP7
PubMed Links
Gene Details
- Gene
- MAP7
- Gene Name
- microtubule associated protein 7
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001198608.1 |
3406 |
Missense Mutation |
AAT,GAT |
N748D |
NP_001185537.1 |
NM_001198609.1 |
3406 |
Missense Mutation |
AAT,GAT |
N756D |
NP_001185538.1 |
NM_001198611.1 |
3406 |
Missense Mutation |
AAT,GAT |
N711D |
NP_001185540.1 |
NM_001198614.1 |
3406 |
Missense Mutation |
AAT,GAT |
N748D |
NP_001185543.1 |
NM_001198615.1 |
3406 |
Missense Mutation |
AAT,GAT |
N711D |
NP_001185544.1 |
NM_001198616.1 |
3406 |
Missense Mutation |
AAT,GAT |
N689D |
NP_001185545.1 |
NM_001198617.1 |
3406 |
Missense Mutation |
AAT,GAT |
N632D |
NP_001185546.1 |
NM_001198618.1 |
3406 |
Missense Mutation |
AAT,GAT |
N580D |
NP_001185547.1 |
NM_001198619.1 |
3406 |
Missense Mutation |
AAT,GAT |
N580D |
NP_001185548.1 |
NM_003980.4 |
3406 |
Missense Mutation |
AAT,GAT |
N726D |
NP_003971.1 |
XM_006715598.2 |
3406 |
Missense Mutation |
AAT,GAT |
N756D |
XP_006715661.1 |
XM_006715599.2 |
3406 |
Missense Mutation |
AAT,GAT |
N756D |
XP_006715662.1 |
XM_006715600.2 |
3406 |
Missense Mutation |
AAT,GAT |
N748D |
XP_006715663.1 |
XM_006715601.3 |
3406 |
Missense Mutation |
AAT,GAT |
N734D |
XP_006715664.1 |
XM_011536243.2 |
3406 |
Missense Mutation |
AAT,GAT |
N719D |
XP_011534545.1 |
XM_011536244.2 |
3406 |
Missense Mutation |
AAT,GAT |
N719D |
XP_011534546.1 |
XM_011536245.1 |
3406 |
Missense Mutation |
AAT,GAT |
N697D |
XP_011534547.1 |
XM_011536246.2 |
3406 |
Missense Mutation |
AAT,GAT |
N682D |
XP_011534548.1 |
XM_017011471.1 |
3406 |
Missense Mutation |
AAT,GAT |
N711D |
XP_016866960.1 |
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