Product Details

SNP ID: rs17092209
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:35004918 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GATGGATCCATGACGCTGCATTAAG[A/G]AAAACAACGCAAAAGTTCCACTCCT
Phenotype: MIM: 609928 MIM: 608430
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MYH7B PubMed Links

Gene Details

Gene: MYH7B
Gene Name: myosin heavy chain 7B

There are no transcripts associated with this gene.

Gene: TRPC4AP
Gene Name: transient receptor potential cation channel subfamily C member 4 associated protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015638.2		Intron			NP_056453.1
NM_199368.1		Intron			NP_955400.1
XM_011528772.2		Intron			XP_011527074.1
XM_011528774.1		Intron			XP_011527076.1
XM_017027799.1		Intron			XP_016883288.1
XM_017027800.1		Intron			XP_016883289.1
XM_017027801.1		Intron			XP_016883290.1

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