Product Details

SNP ID
rs141130793
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:36170982 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTGGTCTTTCAGCTGTGGTCGCC[A/G]GGACCCCCCCAGAGCCAAGACCTTC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MAP7D1 PubMed Links

Gene Details

Gene
MAP7D1
Gene Name
MAP7 domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286365.1 326 Missense Mutation AGG,GGG R20G NP_001273294.1
NM_001286366.1 326 Missense Mutation AGG,GGG R20G NP_001273295.1
NM_018067.4 326 Missense Mutation AGG,GGG R20G NP_060537.3
XM_005271027.1 326 Missense Mutation AGG,GGG R20G XP_005271084.1
XM_006710759.1 326 Missense Mutation AGG,GGG R20G XP_006710822.1
XM_006710761.1 326 Missense Mutation AGG,GGG R20G XP_006710824.1

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