Product Details

SNP ID
rs6914799
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:25279891 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTCCTCTGCGTACTCCTCACCTCT[A/C]TCTCCCTTCCCACCTCTGCTTTCCC
Phenotype
MIM: 609593
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CARMIL1 PubMed Links

Gene Details

Gene
CARMIL1
Gene Name
capping protein regulator and myosin 1 linker 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173977.1 Intron NP_001167448.1
NM_017640.5 Intron NP_060110.4
XM_005249218.1 Intron XP_005249275.1
XM_017011008.1 Intron XP_016866497.1
XM_017011009.1 Intron XP_016866498.1
XM_017011010.1 Intron XP_016866499.1
XM_017011011.1 Intron XP_016866500.1
XM_017011012.1 Intron XP_016866501.1
XM_017011013.1 Intron XP_016866502.1
XM_017011014.1 Intron XP_016866503.1
XM_017011015.1 Intron XP_016866504.1
XM_017011016.1 Intron XP_016866505.1
XM_017011017.1 Intron XP_016866506.1
Gene
LOC105375106
Gene Name
uncharacterized LOC105375106
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_011515047.2 Intron XP_011513349.1

View Full Product Details