Product Details

SNP ID: rs185835285
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:41703367 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAAGCACATGTTGTCCTGCTTCCAA[C/G]ATGCCCTTGTGAGGCATACCTCCCT
Phenotype: MIM: 608797
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: C22orf46 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152513.3	245	Missense Mutation	CAT,GAT	H71D	NP_689726.3
XM_011529935.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528237.1
XM_011529936.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528238.1
XM_011529937.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528239.1
XM_011529938.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528240.1
XM_011529939.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528241.1
XM_011529940.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528242.1
XM_011529941.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528243.1
XM_011529942.2	245	Missense Mutation	CAT,GAT	H7D	XP_011528244.1
XM_011529943.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528245.1
XM_011529944.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528246.1
XM_011529945.2	245	Missense Mutation	CAT,GAT	H71D	XP_011528247.1
XM_011529946.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528248.1
XM_011529947.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528249.1
XM_011529948.2	245	Intron			XP_011528250.1
XM_011529949.1	245	Intron			XP_011528251.1
XM_011529950.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528252.1
XM_011529952.1	245	Intron			XP_011528254.1
XM_011529954.1	245	Intron			XP_011528256.1
XM_011529955.1	245	Missense Mutation	CAT,GAT	H71D	XP_011528257.1
XM_011529956.2	245	Missense Mutation	CAT,GAT	H71D	XP_011528258.1
XM_017028633.1	245	Missense Mutation	CAT,GAT	H71D	XP_016884122.1
XM_017028635.1	245	Intron			XP_016884124.1