Product Details

SNP ID

rs201983608

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:23680267 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCGGCGCGGCGGCGGTGGACGAG[G/T]ACCTGGAGTACCGGAGGTGAGGCTG

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM221A PubMed Links

Gene Details

Gene

FAM221A

Gene Name

family with sequence similarity 221 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127364.2	149	Missense Mutation	GAC,TAC	D17Y	NP_001120836.1
NM_001127365.2	149	Missense Mutation	GAC,TAC	D17Y	NP_001120837.1
NM_001300932.1	149	Missense Mutation	GAC,TAC	D17Y	NP_001287861.1
NM_199136.4	149	Missense Mutation	GAC,TAC	D17Y	NP_954587.2
XM_011515369.2	149	Missense Mutation	GAC,TAC	D17Y	XP_011513671.1
XM_011515370.2	149	Missense Mutation	GAC,TAC	D17Y	XP_011513672.1
XM_011515371.2	149	Missense Mutation	GAC,TAC	D17Y	XP_011513673.1
XM_011515372.2	149	Intron			XP_011513674.1
XM_017012134.1	149	Missense Mutation	GAC,TAC	D17Y	XP_016867623.1
XM_017012135.1	149	Intron			XP_016867624.1

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