Product Details

SNP ID

rs147744090

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:205770795 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGTTTCTGTCCAACCTGTGAAACC[A/G]TTCTCTTTACTGAACCGGTCAATCT

Phenotype

MIM: 603949

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RAB29 PubMed Links

Gene Details

Gene

RAB29

Gene Name

RAB29, member RAS oncogene family

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135662.1	384	Silent Mutation	AAC,AAT	N146N	NP_001129134.1
NM_001135663.1	384	Silent Mutation	AAC,AAT	N122N	NP_001129135.1
NM_001135664.1	384	Silent Mutation	AAC,AAT	N74N	NP_001129136.1
NM_003929.2	384	Silent Mutation	AAC,AAT	N146N	NP_003920.1
XM_005245569.1	384	Silent Mutation	AAC,AAT	N146N	XP_005245626.1
XM_005245570.1	384	Silent Mutation	AAC,AAT	N146N	XP_005245627.1
XM_005245571.1	384	Silent Mutation	AAC,AAT	N146N	XP_005245628.1
XM_006711605.3	384	Silent Mutation	AAC,AAT	N74N	XP_006711668.1
XM_006711606.2	384	Silent Mutation	AAC,AAT	N74N	XP_006711669.1
XM_017002748.1	384	Silent Mutation	AAC,AAT	N122N	XP_016858237.1
XM_017002749.1	384	Silent Mutation	AAC,AAT	N122N	XP_016858238.1
XM_017002750.1	384	Silent Mutation	AAC,AAT	N122N	XP_016858239.1

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