Product Details

SNP ID

rs201603422

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:10490475 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATAACACAAAGACCAGGCTACAGAG[A/G]CAAGAGGTGTCTGGTGAGAGGGAGT

Phenotype

MIM: 611434

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CLNK PubMed Links

Gene Details

Gene

CLNK

Gene Name

cytokine dependent hematopoietic cell linker

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_052964.2	1647	Missense Mutation	CCT,TCT	P427S	NP_443196.2
XM_011513775.2	1647	Missense Mutation	CCT,TCT	P442S	XP_011512077.1
XM_017007684.1	1647	Intron			XP_016863173.1
XM_017007685.1	1647	Intron			XP_016863174.1

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