Product Details

SNP ID
rs150581659
Assay Type
Functionally tested
NCBI dbSNP Submissions
13
Location
Chr.1:16447908 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGGCCCCGGTGGATCAGTTTCCT[A/G]GCACAGCTGTGGAGAGTGTGACGGA
Phenotype
MIM: 611624
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NECAP2 PubMed Links

Gene Details

Gene
NECAP2
Gene Name
NECAP endocytosis associated 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145277.1 322 Missense Mutation AGC,GGC S78G NP_001138749.1
NM_001145278.1 322 Missense Mutation AGC,GGC S52G NP_001138750.1
NM_018090.4 322 Missense Mutation AGC,GGC S78G NP_060560.1
XM_011541767.2 322 Missense Mutation AGC,GGC S25G XP_011540069.1
XM_017001721.1 322 Missense Mutation AGC,GGC S78G XP_016857210.1

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