Product Details

SNP ID

rs7953926

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:23536424 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTAAGTATAACAGGAAGTTTGCCC[C/T]ATGAGAAAAATGACTAAAAGGTACA

Phenotype

MIM: 604975

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SOX5 PubMed Links

Gene Details

Gene

SOX5

Gene Name

SRY-box 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001261414.1		Intron			NP_001248343.1
NM_001261415.1		Intron			NP_001248344.1
NM_006940.4		Intron			NP_008871.3
NM_152989.3		Intron			NP_694534.1
NM_178010.2		Intron			NP_821078.1
XM_011520831.2		Intron			XP_011519133.1
XM_011520832.2		Intron			XP_011519134.1
XM_011520833.2		Intron			XP_011519135.1
XM_011520834.2		Intron			XP_011519136.1
XM_011520835.2		Intron			XP_011519137.1
XM_011520837.2		Intron			XP_011519139.1
XM_011520838.2		Intron			XP_011519140.1
XM_011520842.2		Intron			XP_011519144.1
XM_017019888.1		Intron			XP_016875377.1
XM_017019889.1		Intron			XP_016875378.1
XM_017019890.1		Intron			XP_016875379.1
XM_017019891.1		Intron			XP_016875380.1
XM_017019892.1		Intron			XP_016875381.1
XM_017019893.1		Intron			XP_016875382.1
XM_017019894.1		Intron			XP_016875383.1
XM_017019895.1		Intron			XP_016875384.1
XM_017019896.1		Intron			XP_016875385.1
XM_017019897.1		Intron			XP_016875386.1
XM_017019898.1		Intron			XP_016875387.1
XM_017019899.1		Intron			XP_016875388.1
XM_017019900.1		Intron			XP_016875389.1
XM_017019901.1		Intron			XP_016875390.1
XM_017019902.1		Intron			XP_016875391.1
XM_017019903.1		Intron			XP_016875392.1

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