Product Details

SNP ID

rs61730838

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:22548300 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACAGCACGTGGGTCAGATTGCTCA[A/G]CCCGATGAGGTGCTGCAGGAGACTC

Phenotype

MIM: 606021

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PRAME PubMed Links

Gene Details

Gene

PRAME

Gene Name

preferentially expressed antigen in melanoma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291715.1	1822	Silent Mutation	CTG,TTG	L433L	NP_001278644.1
NM_001291716.1	1822	Silent Mutation	CTG,TTG	L433L	NP_001278645.1
NM_001291717.1	1822	Silent Mutation	CTG,TTG	L417L	NP_001278646.1
NM_001291719.1	1822	Silent Mutation	CTG,TTG	L417L	NP_001278648.1
NM_001318126.1	1822	Silent Mutation	CTG,TTG	L417L	NP_001305055.1
NM_001318127.1	1822	Silent Mutation	CTG,TTG	L417L	NP_001305056.1
NM_006115.4	1822	Silent Mutation	CTG,TTG	L433L	NP_006106.1
NM_206953.2	1822	Silent Mutation	CTG,TTG	L433L	NP_996836.1
NM_206954.2	1822	Silent Mutation	CTG,TTG	L433L	NP_996837.1
NM_206955.2	1822	Silent Mutation	CTG,TTG	L433L	NP_996838.1
NM_206956.2	1822	Silent Mutation	CTG,TTG	L433L	NP_996839.1
XM_011530034.2	1822	Silent Mutation	CTG,TTG	L417L	XP_011528336.1

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