Product Details

SNP ID

rs7886658

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:31120136 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGAGGTAACAGATTTGCAAAATTA[C/T]AGGTCACACGGTGGTATCTATTGAA

Phenotype

MIM: 300377

Polymorphism

C/T, Transition 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	6140	UTR 3			NP_000100.2
NM_004006.2	6140	UTR 3			NP_003997.1
NM_004009.3	6140	UTR 3			NP_004000.1
NM_004010.3	6140	UTR 3			NP_004001.1
NM_004011.3	6140	UTR 3			NP_004002.2
NM_004012.3	6140	UTR 3			NP_004003.1
NM_004013.2	6140	UTR 3			NP_004004.1
NM_004014.2	6140	UTR 3			NP_004005.1
NM_004015.2	6140	UTR 3			NP_004006.1
NM_004016.2	6140	UTR 3			NP_004007.1
NM_004017.2	6140	UTR 3			NP_004008.1
NM_004018.2	6140	UTR 3			NP_004009.1
NM_004019.2	6140	Intron			NP_004010.1
NM_004020.3	6140	UTR 3			NP_004011.2
NM_004021.2	6140	UTR 3			NP_004012.1
NM_004022.2	6140	UTR 3			NP_004013.1
NM_004023.2	6140	UTR 3			NP_004014.1
XM_006724468.2	6140	UTR 3			XP_006724531.1
XM_006724469.3	6140	UTR 3			XP_006724532.1
XM_006724470.3	6140	UTR 3			XP_006724533.1
XM_006724473.2	6140	UTR 3			XP_006724536.1
XM_006724474.3	6140	UTR 3			XP_006724537.1
XM_006724475.2	6140	UTR 3			XP_006724538.1
XM_011545467.1	6140	UTR 3			XP_011543769.1
XM_011545468.2	6140	Intron			XP_011543770.1
XM_011545469.1	6140	Intron			XP_011543771.1
XM_017029328.1	6140	UTR 3			XP_016884817.1
XM_017029329.1	6140	Intron			XP_016884818.1
XM_017029330.1	6140	Intron			XP_016884819.1
XM_017029331.1	6140	UTR 3			XP_016884820.1

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