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SNP ID: rs113262164
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:102726203 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGGAAGCTGAGGCACACATTGGTT[A/G]AGTAGCTTAGCCAACCTCACTGAGT
Phenotype: MIM: 300921
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ARMCX5-GPRASP2 PubMed Links

Gene Details

Gene: ARMCX5-GPRASP2
Gene Name: ARMCX5-GPRASP2 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199818.1		Intron			NP_001186747.1

Gene: BHLHB9
Gene Name: basic helix-loop-helix domain containing, class B, 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142524.1		Intron			NP_001135996.1
NM_001142525.1		Intron			NP_001135997.1
NM_001142526.1		Intron			NP_001135998.1
NM_001142527.1		Intron			NP_001135999.1
NM_001142528.1		Intron			NP_001136000.1
NM_001142529.1		Intron			NP_001136001.1
NM_001142530.1		Intron			NP_001136002.1
NM_030639.2		Intron			NP_085142.1

Gene: GPRASP2
Gene Name: G protein-coupled receptor associated sorting protein 2

There are no transcripts associated with this gene.

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