Product Details

SNP ID

rs11950502

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:74777759 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCAGGAAACAATCACAAAATATAG[C/G]TTTAATTACTACTTTTAAACTTAAA

Phenotype

MIM: 615769 MIM: 612497

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM169A PubMed Links

Gene Details

Gene

FAM169A

Gene Name

family with sequence similarity 169 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015566.2	6027	UTR 3			NP_056381.1
XM_005248480.2	6027	UTR 3			XP_005248537.1
XM_011543306.2	6027	UTR 3			XP_011541608.1
XM_011543307.2	6027	UTR 3			XP_011541609.1
XM_017009332.1	6027	UTR 3			XP_016864821.1
XM_017009333.1	6027	UTR 3			XP_016864822.1

Gene

NSA2

Gene Name

NSA2, ribosome biogenesis homolog

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271665.1	6027	Intron			NP_001258594.1
NM_014886.4	6027	Intron			NP_055701.1
XM_011543098.1	6027	Intron			XP_011541400.1
XM_017008952.1	6027	Intron			XP_016864441.1
XM_017008953.1	6027	Intron			XP_016864442.1

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