Product Details

SNP ID

rs140222626

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:49256847 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGTAGGAGCTCTGGGGCACAGCC[A/G]AAAGGGTGCTGGGGGGACAGAGGGT

Phenotype

MIM: 300859 MIM: 300292

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

CCDC22 PubMed Links

Gene Details

Gene

CCDC22

Gene Name

coiled-coil domain containing 22

There are no transcripts associated with this gene.

Gene

FOXP3

Gene Name

forkhead box P3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114377.1	739	Missense Mutation	TCG,TTG	S149L	NP_001107849.1
NM_014009.3	739	Missense Mutation	TCG,TTG	S184L	NP_054728.2
XM_006724533.2	739	Missense Mutation	TCG,TTG	S207L	XP_006724596.2
XM_011543916.2	739	Missense Mutation	TCG,TTG	S257L	XP_011542218.1
XM_017029565.1	739	Missense Mutation	TCG,TTG	S269L	XP_016885054.1
XM_017029566.1	739	Missense Mutation	TCG,TTG	S257L	XP_016885055.1
XM_017029567.1	739	Missense Mutation	TCG,TTG	S166L	XP_016885056.1

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