Product Details

SNP ID

rs34318529

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:718586 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAGGCAACAGGTTTGCTTCTCTGC[G/A]TCTGTGGCCTGCTTTGACCTCCGTC

Phenotype

MIM: 608134

Polymorphism

G/A, Transition substitution

Allele Nomenclature

Literature Links

PALM PubMed Links

Gene Details

Gene

PALM

Gene Name

paralemmin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040134.1		Intron			NP_001035224.1
NM_002579.2		Intron			NP_002570.2
XM_005259565.4		Intron			XP_005259622.1
XM_005259566.4		Intron			XP_005259623.1
XM_017026850.1		Intron			XP_016882339.1

View Full Product Details