Product Details

SNP ID

rs143641709

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:37943061 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACAGGGCCGTTTTATTCTGCAAAC[C/T]GAAACTTGGGTCATGTGACCTGATG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C22orf23 PubMed Links

Gene Details

Gene

C22orf23

Gene Name

chromosome 22 open reading frame 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001207062.1	1766	UTR 3			NP_001193991.1
NM_032561.4	1766	UTR 3			NP_115950.3
XM_005261781.1	1766	Intron			XP_005261838.1
XM_005261782.3	1766	Intron			XP_005261839.1
XM_005261783.2	1766	Intron			XP_005261840.1
XM_005261784.2	1766	Intron			XP_005261841.1

Gene

MICALL1

Gene Name

MICAL like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033386.3	1766	Intron			NP_203744.1
XM_005261791.3	1766	Intron			XP_005261848.1
XM_005261792.3	1766	Intron			XP_005261849.1
XM_011530471.2	1766	Intron			XP_011528773.1
XM_011530472.2	1766	Intron			XP_011528774.1
XM_011530473.2	1766	Intron			XP_011528775.1
XM_011530474.2	1766	Intron			XP_011528776.1
XM_011530475.2	1766	Intron			XP_011528777.1
XM_011530476.2	1766	Intron			XP_011528778.1
XM_017029026.1	1766	Intron			XP_016884515.1

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