Product Details

SNP ID
rs1132357
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:24804548 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTAACATAAGCTATAGGCTATACCT[A/C]CTAACTACAGACTGTACAATGTACC
Phenotype
MIM: 611410
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
C6orf229 PubMed Links

Gene Details

Gene
C6orf229
Gene Name
chromosome 6 open reading frame 229
There are no transcripts associated with this gene.

Gene
FAM65B
Gene Name
family with sequence similarity 65 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286445.1 5318 UTR 3 NP_001273374.1
NM_001286446.1 5318 Intron NP_001273375.1
NM_001286447.1 5318 Intron NP_001273376.1
NM_014722.3 5318 UTR 3 NP_055537.2
NM_015864.3 5318 Intron NP_056948.2
XM_006715275.2 5318 UTR 3 XP_006715338.1
XM_006715277.1 5318 UTR 3 XP_006715340.1
XM_006715279.2 5318 UTR 3 XP_006715342.1
XM_006715281.3 5318 Intron XP_006715344.1
XM_011515007.1 5318 UTR 3 XP_011513309.1
XM_011515008.2 5318 UTR 3 XP_011513310.1
XM_011515009.1 5318 UTR 3 XP_011513311.1
XM_011515010.2 5318 UTR 3 XP_011513312.1
XM_011515012.1 5318 UTR 3 XP_011513314.1
XM_017011523.1 5318 UTR 3 XP_016867012.1
XM_017011524.1 5318 Intron XP_016867013.1
XM_017011525.1 5318 Intron XP_016867014.1
XM_017011526.1 5318 Intron XP_016867015.1
XM_017011527.1 5318 Intron XP_016867016.1

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