Product Details

SNP ID

rs13333

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:37591551 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATAACTAACCAGTTGTTCAACAGC[A/G]GGTTAAGCTCAGCAGTTTTCACAGT

Phenotype

MIM: 611212

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C4orf19 PubMed Links

Gene Details

Gene

C4orf19

Gene Name

chromosome 4 open reading frame 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001104629.1	1743	UTR 3			NP_001098099.1
NM_018302.2	1743	UTR 3			NP_060772.2
XM_011513712.2	1743	UTR 3			XP_011512014.1
XM_011513713.2	1743	UTR 3			XP_011512015.1
XM_017008361.1	1743	UTR 3			XP_016863850.1

Gene

RELL1

Gene Name

RELT like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001085399.1	1743	Intron			NP_001078868.1
NM_001085400.1	1743	Intron			NP_001078869.1
XM_017008590.1	1743	Intron			XP_016864079.1

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