Product Details

SNP ID

rs3177555

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:1292391 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCACGGGAGCCCAGGAGCAGGCAG[T/G]GGGCGCAAGTGCTTTATTCAAAGCG

Phenotype

MIM: 601328

Polymorphism

T/G, Transversion substitution

Allele Nomenclature

Literature Links

ACAP3 PubMed Links

Gene Details

Gene

ACAP3

Gene Name

ArfGAP with coiled-coil, ankyrin repeat and PH domains 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030649.2	6225	UTR 3			NP_085152.2
XM_005244715.2	6225	UTR 3			XP_005244772.1
XM_005244717.3	6225	UTR 3			XP_005244774.1
XM_011540606.2	6225	UTR 3			XP_011538908.1
XM_011540607.1	6225	UTR 3			XP_011538909.1
XM_011540608.2	6225	UTR 3			XP_011538910.1
XM_011540609.2	6225	UTR 3			XP_011538911.1
XM_017000233.1	6225	UTR 3			XP_016855722.1

Gene

MIR6726

Gene Name

microRNA 6726

There are no transcripts associated with this gene.

Gene

SCNN1D

Gene Name

sodium channel epithelial 1 delta subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130413.3	6225	Intron			NP_001123885.2
XM_011541899.2	6225	Intron			XP_011540201.1
XM_011541901.2	6225	Intron			XP_011540203.1
XM_011541902.2	6225	Intron			XP_011540204.1
XM_011541905.2	6225	Intron			XP_011540207.1
XM_011541906.2	6225	Intron			XP_011540208.1
XM_011541908.2	6225	Intron			XP_011540210.1
XM_011541920.2	6225	Intron			XP_011540222.1
XM_011541925.2	6225	Intron			XP_011540227.1
XM_011541929.2	6225	Intron			XP_011540231.1
XM_011541932.2	6225	Intron			XP_011540234.1
XM_011541933.2	6225	Intron			XP_011540235.1
XM_017002037.1	6225	Intron			XP_016857526.1
XM_017002038.1	6225	Intron			XP_016857527.1
XM_017002039.1	6225	Intron			XP_016857528.1
XM_017002040.1	6225	Intron			XP_016857529.1
XM_017002041.1	6225	Intron			XP_016857530.1
XM_017002042.1	6225	Intron			XP_016857531.1
XM_017002043.1	6225	Intron			XP_016857532.1
XM_017002044.1	6225	Intron			XP_016857533.1

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