Product Details

SNP ID

rs738980

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:32511375 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GGGGGTCTAGAAGAATGTGTCGACA[A/G]TGATGCCTGCAAAGCAGCAGCTTCA

Phenotype

MIM: 602705

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SYN3 PubMed Links

Gene Details

Gene

SYN3

Gene Name

synapsin III

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135774.1	4728	Intron			NP_001129246.1
NM_003490.3	4728	Intron			NP_003481.3
NM_133633.2	4728	Intron			NP_598344.2
XM_011530405.2	4728	UTR 3			XP_011528707.1
XM_011530406.2	4728	UTR 3			XP_011528708.1
XM_011530407.2	4728	UTR 3			XP_011528709.1
XM_011530408.1	4728	UTR 3			XP_011528710.1
XM_011530410.2	4728	UTR 3			XP_011528712.1
XM_017028960.1	4728	UTR 3			XP_016884449.1
XM_017028961.1	4728	UTR 3			XP_016884450.1
XM_017028962.1	4728	UTR 3			XP_016884451.1
XM_017028963.1	4728	UTR 3			XP_016884452.1
XM_017028964.1	4728	UTR 3			XP_016884453.1
XM_017028965.1	4728	UTR 3			XP_016884454.1

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