Product Details

SNP ID

rs12632822

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:197889892 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

GATGCTCTCCTGTCGTGCAGGACCC[G/A]GAGCTTAAGCCATGGACTCAAGAGT

Phenotype

MIM: 612477

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

IQCG PubMed Links

Gene Details

Gene

IQCG

Gene Name

IQ motif containing G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134435.2		Intron			NP_001127907.1
NM_001323027.1		Intron			NP_001309956.1
NM_001323028.1		Intron			NP_001309957.1
NM_001323029.1		Intron			NP_001309958.1
NM_001323030.1		Intron			NP_001309959.1
NM_032263.4		Intron			NP_115639.1
XM_017007316.1		Intron			XP_016862805.1
XM_017007317.1		Intron			XP_016862806.1

Gene

LRCH3

Gene Name

leucine rich repeats and calponin homology domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032773.3		Intron			NP_116162.1
XM_005269362.2		Intron			XP_005269419.1
XM_005269363.2		Intron			XP_005269420.1
XM_005269365.2		Intron			XP_005269422.1
XM_005269367.2		Intron			XP_005269424.1
XM_006713791.3		Intron			XP_006713854.1
XM_006713792.3		Intron			XP_006713855.1
XM_006713793.2		Intron			XP_006713856.1
XM_011513242.2		Intron			XP_011511544.1
XM_011513243.2		Intron			XP_011511545.1
XM_017007350.1		Intron			XP_016862839.1
XM_017007351.1		Intron			XP_016862840.1
XM_017007352.1		Intron			XP_016862841.1

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