Product Details

SNP ID: rs183487896
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:41690609 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGCCCTCTAGCTCCCAACACCATCT[A/G]CCTGATCTAAGCTTTGCCATGTTGT
Phenotype: MIM: 608797 MIM: 601304
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C22orf46 PubMed Links

Gene Details

Gene: C22orf46
Gene Name: chromosome 22 open reading frame 46

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142964.1	67	UTR 5			NP_001136436.1
XM_011530373.2	67	UTR 5			XP_011528675.1
XM_017028939.1	67	Intron			XP_016884428.1

Gene: MEI1
Gene Name: meiotic double-stranded break formation protein 1

There are no transcripts associated with this gene.

Gene: SNU13
Gene Name: SNU13 homolog, small nuclear ribonucleoprotein (U4/U6.U5)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003796.1	67	Intron			NP_001003796.1
NM_005008.3	67	Intron			NP_004999.1
XM_017028811.1	67	Intron			XP_016884300.1

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