Product Details

SNP ID

rs11995

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:20781764 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGATCAACAGTTGACAGTTAGTTG[C/T]GAGGAAAGGGTCCAAAAGGCATGGA

Phenotype

MIM: 605491

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NEBL PubMed Links

Additional Information

For this assay, SNP(s) [rs78806491] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NEBL

Gene Name

nebulette

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001173484.1	7421	UTR 3			NP_001166955.1
NM_006393.2	7421	UTR 3			NP_006384.1
NM_213569.2	7421	UTR 3			NP_998734.1
XM_005252342.4	7421	UTR 3			XP_005252399.1
XM_005252343.4	7421	UTR 3			XP_005252400.1
XM_005252344.4	7421	UTR 3			XP_005252401.1
XM_011519291.2	7421	UTR 3			XP_011517593.1
XM_017015467.1	7421	UTR 3			XP_016870956.1
XM_017015468.1	7421	UTR 3			XP_016870957.1
XM_017015469.1	7421	Intron			XP_016870958.1

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