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See other MYO19 GT Assays ›
SNP ID:
rs78083058
Gene
MYO19 ZNHIT3
Gene Name
Set Membership:
-
Chromosome Location:
Chr.17: 36501152 - 36501152 on Build GRCh38
Polymorphism:
C/G, Transversion substitution
Context Sequence [VIC/FAM]:

TCAGCCGAGTCACCAGTTATGGCTG[C/G]TGCCTGAGTTAGGACCGGCAGAGTG

Assay ID C_102227283_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 604500

Literature Links:

 MYO19 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
MYO19 - myosin XIX
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001033580.2 2817 Intron NP_001028752.1
NM_001163735.1 2817 Missense Mutation CCA,GCA P,A 722 NP_001157207.1
NM_025109.5 2817 Missense Mutation CCA,GCA P,A 522 NP_079385.2
XM_011525286.1 2817 Missense Mutation CCA,GCA P,A 799 XP_011523588.1
XM_011525287.1 2817 Missense Mutation CCA,GCA P,A 797 XP_011523589.1
XM_011525290.2 2817 Missense Mutation CCA,GCA P,A 753 XP_011523592.1
XM_017025157.1 2817 Missense Mutation CCA,GCA P,A 799 XP_016880646.1
XM_017025158.1 2817 Missense Mutation CCA,GCA P,A 768 XP_016880647.1
XM_017025159.1 2817 Missense Mutation CCA,GCA P,A 755 XP_016880648.1
XM_017025160.1 2817 Missense Mutation CCA,GCA P,A 799 XP_016880649.1
XM_017025161.1 2817 Missense Mutation CCA,GCA P,A 606 XP_016880650.1
ZNHIT3 - zinc finger HIT-type containing 3
There are no transcripts associated with this gene.

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