Product Details

SNP ID
rs148121639
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48295132 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCGAAACTCCCACGGATAGAAT[A/C]TGGGGCCACATGGCGTGCTCGGAAC
Phenotype
MIM: 608294
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
FCF1P2 PubMed Links

Gene Details

Gene
FCF1P2
Gene Name
FCF1 pseudogene 2
There are no transcripts associated with this gene.

Gene
NME6
Gene Name
NME/NM23 nucleoside diphosphate kinase 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308426.1 677 Missense Mutation NP_001295355.1
NM_001308427.1 677 Missense Mutation NP_001295356.1
NM_001308428.1 677 Missense Mutation NP_001295357.1
NM_001308430.1 677 Missense Mutation NP_001295359.1
NM_001308431.1 677 Missense Mutation NP_001295360.1
NM_001308433.1 677 Missense Mutation NP_001295362.1
NM_001308434.1 677 Missense Mutation NP_001295363.1
NM_001308435.1 677 Intron NP_001295364.1
NM_005793.4 677 Missense Mutation NP_005784.1
XM_017005511.1 677 Missense Mutation XP_016861000.1
XM_017005512.1 677 Intron XP_016861001.1
XM_017005513.1 677 Missense Mutation XP_016861002.1
XM_017005514.1 677 Missense Mutation XP_016861003.1
XM_017005515.1 677 Missense Mutation XP_016861004.1
XM_017005516.1 677 Missense Mutation XP_016861005.1
XM_017005517.1 677 Missense Mutation XP_016861006.1
XM_017005518.1 677 Missense Mutation XP_016861007.1

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