Product Details

SNP ID
rs5926985
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:31124177 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTACACTGCTGCATTTTCACAAATG[A/C]CCTTGTGGCCATCTTTGTGCTATAA
Phenotype
MIM: 300377
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
DMD PubMed Links

Gene Details

Gene
DMD
Gene Name
dystrophin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000109.3 Intron NP_000100.2
NM_004006.2 Intron NP_003997.1
NM_004009.3 Intron NP_004000.1
NM_004010.3 Intron NP_004001.1
NM_004011.3 Intron NP_004002.2
NM_004012.3 Intron NP_004003.1
NM_004013.2 Intron NP_004004.1
NM_004014.2 Intron NP_004005.1
NM_004015.2 Intron NP_004006.1
NM_004016.2 Intron NP_004007.1
NM_004017.2 Intron NP_004008.1
NM_004018.2 Intron NP_004009.1
NM_004019.2 Intron NP_004010.1
NM_004020.3 Intron NP_004011.2
NM_004021.2 Intron NP_004012.1
NM_004022.2 Intron NP_004013.1
NM_004023.2 Intron NP_004014.1

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