Product Details

SNP ID

rs114902483

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:45335976 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTATGGAGATACTACTTACAAAGAC[A/G]ATGTGCTACAGTGTATTTCTAAAGA

Phenotype

MIM: 600211 MIM: 602947

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RUNX2 PubMed Links

Gene Details

Gene

RUNX2

Gene Name

runt related transcription factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001015051.3		Intron			NP_001015051.3
NM_001024630.3		Intron			NP_001019801.3
NM_001278478.1		Intron			NP_001265407.1
XM_006715232.1		Intron			XP_006715295.1
XM_011514960.2		Intron			XP_011513262.1
XM_011514961.2		Intron			XP_011513263.1
XM_011514962.2		Intron			XP_011513264.1
XM_011514963.2		Intron			XP_011513265.1
XM_011514964.2		Intron			XP_011513266.1
XM_011514965.2		Intron			XP_011513267.1
XM_011514966.2		Intron			XP_011513268.1
XM_017011391.1		Intron			XP_016866880.1
XM_017011392.1		Intron			XP_016866881.1
XM_017011393.1		Intron			XP_016866882.1
XM_017011394.1		Intron			XP_016866883.1
XM_017011395.1		Intron			XP_016866884.1
XM_017011396.1		Intron			XP_016866885.1

Gene

SUPT3H

Gene Name

SPT3 homolog, SAGA and STAGA complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001261823.1		Intron			NP_001248752.1
NM_003599.3		Intron			NP_003590.1
NM_181356.2		Intron			NP_852001.1
XM_011514949.2		Intron			XP_011513251.1
XM_011514950.1		Intron			XP_011513252.1
XM_011514951.2		Intron			XP_011513253.1
XM_011514952.2		Intron			XP_011513254.1
XM_011514953.2		Intron			XP_011513255.1
XM_011514954.2		Intron			XP_011513256.1
XM_017011369.1		Intron			XP_016866858.1
XM_017011370.1		Intron			XP_016866859.1
XM_017011371.1		Intron			XP_016866860.1
XM_017011372.1		Intron			XP_016866861.1
XM_017011373.1		Intron			XP_016866862.1
XM_017011374.1		Intron			XP_016866863.1

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