Product Details

SNP ID

rs193036151

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:38346459 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTCCCTCCTTGGCAGCTCTTCAAC[C/T]TGATGCCCCAGTACTTTGTGGGTGT

Phenotype

MIM: 613452

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CATSPERG PubMed Links

Gene Details

Gene

CATSPERG

Gene Name

cation channel sperm associated auxiliary subunit gamma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021185.4	1382	Silent Mutation	CTG,TTG	L227L	NP_067008.3
XM_005259114.4	1382	Silent Mutation	CTG,TTG	L227L	XP_005259171.1
XM_005259115.4	1382	Silent Mutation	CTG,TTG	L227L	XP_005259172.1
XM_005259116.2	1382	Silent Mutation	CTG,TTG	L227L	XP_005259173.1
XM_006723308.3	1382	Silent Mutation	CTG,TTG	L227L	XP_006723371.1
XM_006723310.2	1382	Silent Mutation	CTG,TTG	L227L	XP_006723373.1
XM_006723311.2	1382	Silent Mutation	CTG,TTG	L227L	XP_006723374.1
XM_011527174.2	1382	Silent Mutation	CTG,TTG	L227L	XP_011525476.1
XM_011527175.2	1382	Silent Mutation	CTG,TTG	L204L	XP_011525477.1
XM_011527176.2	1382	Silent Mutation	CTG,TTG	L227L	XP_011525478.1
XM_011527177.2	1382	Silent Mutation	CTG,TTG	L187L	XP_011525479.1
XM_011527178.2	1382	Silent Mutation	CTG,TTG	L112L	XP_011525480.1
XM_011527179.1	1382	Silent Mutation	CTG,TTG	L227L	XP_011525481.1
XM_011527182.2	1382	UTR 5			XP_011525484.1
XM_017027053.1	1382	Silent Mutation	CTG,TTG	L227L	XP_016882542.1
XM_017027054.1	1382	Silent Mutation	CTG,TTG	L112L	XP_016882543.1
XM_017027055.1	1382	Intron			XP_016882544.1

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