Product Details

SNP ID

rs409874

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:31122045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCATTTCTGGGTGAAGACAACACA[C/G]AAGCTGCATCGAGGGTGTACACAAC

Phenotype

MIM: 300377

Polymorphism

C/G, 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
XM_006724468.2		Intron			XP_006724531.1
XM_006724469.3		Intron			XP_006724532.1
XM_006724470.3		Intron			XP_006724533.1
XM_006724473.2		Intron			XP_006724536.1
XM_006724474.3		Intron			XP_006724537.1
XM_006724475.2		Intron			XP_006724538.1
XM_011545467.1		Intron			XP_011543769.1
XM_011545468.2		Intron			XP_011543770.1
XM_011545469.1		Intron			XP_011543771.1
XM_017029328.1		Intron			XP_016884817.1
XM_017029329.1		Intron			XP_016884818.1
XM_017029330.1		Intron			XP_016884819.1
XM_017029331.1		Intron			XP_016884820.1

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