Product Details

SNP ID

rs61732857

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:101689383 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGGGTCGCTTTTGGCTCCTCGGA[C/T]GAACTCTTCCAGGGAGAGTTTTCCT

Phenotype

MIM: 606722

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NCALD PubMed Links

Gene Details

Gene

NCALD

Gene Name

neurocalcin delta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040624.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035714.1
NM_001040625.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035715.1
NM_001040626.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035716.1
NM_001040627.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035717.1
NM_001040628.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035718.1
NM_001040629.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035719.1
NM_001040630.1	877	Missense Mutation	ATC,GTC	I170V	NP_001035720.1
NM_032041.2	877	Missense Mutation	ATC,GTC	I170V	NP_114430.2
XM_011517332.2	877	Missense Mutation	ATC,GTC	I170V	XP_011515634.1
XM_011517333.2	877	Missense Mutation	ATC,GTC	I170V	XP_011515635.1
XM_011517334.2	877	Missense Mutation	ATC,GTC	I170V	XP_011515636.1
XM_011517335.2	877	Missense Mutation	ATC,GTC	I170V	XP_011515637.1
XM_017013900.1	877	Intron			XP_016869389.1
XM_017013901.1	877	Missense Mutation	ATC,GTC	I170V	XP_016869390.1
XM_017013902.1	877	Missense Mutation	ATC,GTC	I170V	XP_016869391.1

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