Product Details

SNP ID: rs6503190
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:9252737 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTCTGATGATCCAATCTTTTGAGA[A/G]ACGCTTCTCTTGGGGCCCCAAGGTT
Phenotype: MIM: 601614 MIM: 604203
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: NTN1 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004853.2		Intron			NP_004844.1
XM_011524079.2		Intron			XP_011522381.1