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SNP ID: rs111363194
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:155071542 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCGGGCCAAGATGGCGGTGCAGGT[A/G]GTGCAGGCGGTGCAGGCGGTTCATC
Phenotype: MIM: 300617 MIM: 300116
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: BRCC3 PubMed Links

Gene Details

Gene: BRCC3
Gene Name: BRCA1/BRCA2-containing complex subunit 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018055.2	133	Intron			NP_001018065.1
NM_001242640.1	133	Intron			NP_001229569.1
NM_024332.3	133	Intron			NP_077308.1
XM_005274751.4	133	Silent Mutation	GTA,GTG	V5V	XP_005274808.1
XM_017029838.1	133	Intron			XP_016885327.1

Gene: CMC4
Gene Name: C-X9-C motif containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018024.2	133	Intron			NP_001018024.1

Gene: MTCP1
Gene Name: mature T-cell proliferation 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001018025.3	133	Intron			NP_001018025.1

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