Product Details

SNP ID
rs739136
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.22:41704271 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TTTCAGGCTTTTAACTGCCAAGACA[A/G]TTTTTAAGGGAGCTAGGATGATCTC
Phenotype
MIM: 608797
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C22orf46 PubMed Links

Gene Details

Gene
C22orf46
Gene Name
chromosome 22 open reading frame 46
There are no transcripts associated with this gene.

Gene
MEI1
Gene Name
meiotic double-stranded break formation protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152513.3 Intron NP_689726.3
XM_011529935.1 Intron XP_011528237.1
XM_011529936.1 Intron XP_011528238.1
XM_011529937.1 Intron XP_011528239.1
XM_011529938.1 Intron XP_011528240.1
XM_011529939.1 Intron XP_011528241.1
XM_011529940.1 Intron XP_011528242.1
XM_011529941.1 Intron XP_011528243.1
XM_011529942.2 Intron XP_011528244.1
XM_011529943.1 Intron XP_011528245.1
XM_011529944.1 Intron XP_011528246.1
XM_011529945.2 Intron XP_011528247.1
XM_011529946.1 Intron XP_011528248.1
XM_011529947.1 Intron XP_011528249.1
XM_011529948.2 Intron XP_011528250.1
XM_011529949.1 Intron XP_011528251.1
XM_011529950.1 Intron XP_011528252.1
XM_011529952.1 Intron XP_011528254.1
XM_011529954.1 Intron XP_011528256.1
XM_011529955.1 Intron XP_011528257.1
XM_011529956.2 Intron XP_011528258.1
XM_017028633.1 Intron XP_016884122.1
XM_017028635.1 Intron XP_016884124.1

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