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SNP ID: rs138756182
Assay Type: Functionally tested
NCBI dbSNP Submissions: 13
Location: Chr.1:112701679 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTAGCCAAAGGCACTGATCCGGTTC[A/G]CCATGTCCCGGCCTTCCTCAGACCG
Phenotype: MIM: 610742 MIM: 609957 MIM: 165380
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MOV10 PubMed Links

Gene Details

Gene: MOV10
Gene Name: Mov10 RISC complex RNA helicase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130079.2	4634	Intron			NP_001123551.1
NM_001286072.1	4634	Intron			NP_001273001.1
NM_001321324.1	4634	Intron			NP_001308253.1
NM_020963.4	4634	Intron			NP_066014.1
XM_005270869.4	4634	UTR 3			XP_005270926.1
XM_005270870.4	4634	UTR 3			XP_005270927.1
XM_017001318.1	4634	UTR 3			XP_016856807.1
XM_017001319.1	4634	Intron			XP_016856808.1

Gene: PPM1J
Gene Name: protein phosphatase, Mg2+/Mn2+ dependent 1J

There are no transcripts associated with this gene.

Gene: RHOC
Gene Name: ras homolog family member C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042678.1	4634	Missense Mutation	GCG,GTG	A148V	NP_001036143.1
NM_001042679.1	4634	Missense Mutation	GCG,GTG	A148V	NP_001036144.1
NM_175744.4	4634	Missense Mutation	GCG,GTG	A148V	NP_786886.1

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