Product Details

SNP ID

rs1043564

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16518143 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCACCAGGCTGCCCATGGACACCA[C/G]GTGTGGCCGATTCCCAACGGTCACC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C19orf44 PubMed Links

Gene Details

Gene

C19orf44

Gene Name

chromosome 19 open reading frame 44

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001288834.1	3841	UTR 3			NP_001275763.1
NM_032207.3	3841	Intron			NP_115583.1
XM_006722920.3	3841	Intron			XP_006722983.1
XM_011528354.2	3841	UTR 3			XP_011526656.1
XM_017027350.1	3841	Intron			XP_016882839.1

Gene

CHERP

Gene Name

calcium homeostasis endoplasmic reticulum protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006387.5	3841	UTR 3			NP_006378.3

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