Product Details

SNP ID

rs140149

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:29789624 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GATGTGACCTAGGGCCCTTTCAGAC[C/T]ATCTTGACCACTGGGATTTGCCAGA

Phenotype

MIM: 614216

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ASCC2 PubMed Links

Gene Details

Gene

ASCC2

Gene Name

activating signal cointegrator 1 complex subunit 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001242906.1		Intron			NP_001229835.1
NM_032204.4		Intron			NP_115580.2
XM_005261775.2		Intron			XP_005261832.1
XM_011530442.2		Intron			XP_011528744.1
XM_011530443.2		Intron			XP_011528745.1
XM_011530444.2		Intron			XP_011528746.1
XM_011530445.2		Intron			XP_011528747.1
XM_011530446.2		Intron			XP_011528748.1
XM_011530448.2		Intron			XP_011528750.1
XM_011530449.2		Intron			XP_011528751.1
XM_011530450.2		Intron			XP_011528752.1
XM_011530451.2		Intron			XP_011528753.1
XM_011530452.2		Intron			XP_011528754.1
XM_011530453.2		Intron			XP_011528755.1
XM_011530454.2		Intron			XP_011528756.1
XM_011530455.2		Intron			XP_011528757.1
XM_017028991.1		Intron			XP_016884480.1
XM_017028992.1		Intron			XP_016884481.1
XM_017028993.1		Intron			XP_016884482.1
XM_017028994.1		Intron			XP_016884483.1
XM_017028995.1		Intron			XP_016884484.1
XM_017028996.1		Intron			XP_016884485.1
XM_017028997.1		Intron			XP_016884486.1
XM_017028998.1		Intron			XP_016884487.1
XM_017028999.1		Intron			XP_016884488.1
XM_017029000.1		Intron			XP_016884489.1
XM_017029001.1		Intron			XP_016884490.1
XM_017029002.1		Intron			XP_016884491.1
XM_017029003.1		Intron			XP_016884492.1
XM_017029004.1		Intron			XP_016884493.1
XM_017029005.1		Intron			XP_016884494.1
XM_017029006.1		Intron			XP_016884495.1
XM_017029007.1		Intron			XP_016884496.1
XM_017029008.1		Intron			XP_016884497.1
XM_017029009.1		Intron			XP_016884498.1

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