Product Details

SNP ID
rs6051373
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:348315 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACGGTCCTTCGCTTTCAGTCTCTGC[A/C]TTTTCCCGTTCTCTGTCGTGGCTTT
Phenotype
MIM: 610666
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
LOC101929937 PubMed Links

Gene Details

Gene
LOC101929937
Gene Name
uncharacterized LOC101929937
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_017028182.1 432 Missense Mutation AAG,AAT K144N XP_016883671.1
Gene
NRSN2
Gene Name
neurensin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323679.1 432 Intron NP_001310608.1
NM_001323680.1 432 Intron NP_001310609.1
NM_001323681.1 432 Intron NP_001310610.1
NM_001323682.1 432 Intron NP_001310611.1
NM_001323683.1 432 Intron NP_001310612.1
NM_001323684.1 432 Intron NP_001310613.1
NM_001323685.1 432 Intron NP_001310614.1
NM_024958.2 432 Intron NP_079234.1
XM_006723630.3 432 UTR 5 XP_006723693.1
XM_011529360.1 432 Intron XP_011527662.1
XM_011529362.2 432 Intron XP_011527664.1
XM_011529363.2 432 UTR 5 XP_011527665.1
XM_017028073.1 432 Intron XP_016883562.1
XM_017028074.1 432 Intron XP_016883563.1
XM_017028075.1 432 Intron XP_016883564.1
XM_017028076.1 432 Intron XP_016883565.1

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