Product Details

SNP ID

rs201841970

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:97024287 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGTACCTGGCTGGTTGGTGGCGC[C/T]TGGGACGCGGTTGTAGGCGCCGCCG

Phenotype

MIM: 600028

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DLX5 PubMed Links

Gene Details

Gene

DLX5

Gene Name

distal-less homeobox 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005221.5	545	Missense Mutation	AGC,GGC	S113G	NP_005212.1
XM_005250185.3	545	Intron			XP_005250242.1
XM_017011803.1	545	Intron			XP_016867292.1

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