Product Details

SNP ID

rs148130830

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:35618045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTCAACAAGGAGTTGAAGGTGTC[A/C]CGGACCGTGAGTGAGTGACCACGGC

Phenotype

MIM: 610172

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SPEF2 PubMed Links

Gene Details

Gene

SPEF2

Gene Name

sperm flagellar 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024867.3	268	Silent Mutation	TCA,TCC	S16S	NP_079143.3
NM_144722.3	268	Silent Mutation	TCA,TCC	S16S	NP_653323.1
XM_005248376.3	268	Silent Mutation	TCA,TCC	S16S	XP_005248433.1
XM_005248377.3	268	Silent Mutation	TCA,TCC	S16S	XP_005248434.1
XM_005248378.3	268	Silent Mutation	TCA,TCC	S16S	XP_005248435.1
XM_011514135.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512437.1
XM_011514136.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512438.1
XM_011514137.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512439.1
XM_011514138.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512440.1
XM_011514139.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512441.1
XM_011514140.2	268	Silent Mutation	TCA,TCC	S16S	XP_011512442.1
XM_011514141.2	268	UTR 5			XP_011512443.1
XM_011514142.1	268	Silent Mutation	TCA,TCC	S16S	XP_011512444.1
XM_017009880.1	268	Silent Mutation	TCA,TCC	S16S	XP_016865369.1
XM_017009881.1	268	UTR 5			XP_016865370.1
XM_017009882.1	268	Silent Mutation	TCA,TCC	S16S	XP_016865371.1

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