Product Details

SNP ID

rs7760794

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:148200305 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTCTTTAGAACTCTAGCCTGAAAC[A/G]TTGGTTCAGCTAGTCTGTCTTGAAT

Phenotype

MIM: 607955

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SASH1 PubMed Links

Additional Information

For this assay, SNP(s) [rs78496063] 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

SASH1

Gene Name

SAM and SH3 domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015278.3		Intron			NP_056093.3
XM_005266875.1		Intron			XP_005266932.1
XM_011535640.1		Intron			XP_011533942.1
XM_017010598.1		Intron			XP_016866087.1
XM_017010599.1		Intron			XP_016866088.1
XM_017010600.1		Intron			XP_016866089.1
XM_017010601.1		Intron			XP_016866090.1
XM_017010602.1		Intron			XP_016866091.1
XM_017010603.1		Intron			XP_016866092.1
XM_017010604.1		Intron			XP_016866093.1
XM_017010605.1		Intron			XP_016866094.1
XM_017010606.1		Intron			XP_016866095.1
XM_017010607.1		Intron			XP_016866096.1

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