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SNP ID

rs236728

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:58984410 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGACTGAGACTTCAGGGGAATGTTG[C/G]TACTGCAAGCATACAAAAAATAAGG

Phenotype

MIM: 605297

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NELFCD PubMed Links

Gene Details

Gene

NELFCD

Gene Name

negative elongation factor complex member C/D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198976.2		Intron			NP_945327.2

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