Product Details

SNP ID

rs138121177

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:150997633 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGCAGCAGCCCACCTGCAGTGA[C/T]AGGACCCGCGTCCGCATCCGCACTG

Phenotype

MIM: 603319

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ANXA9 PubMed Links

Gene Details

Gene

ANXA9

Gene Name

annexin A9

There are no transcripts associated with this gene.

Gene

FAM63A

Gene Name

family with sequence similarity 63 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040217.2	2000	Silent Mutation	CTA,CTG	L298L	NP_001035307.1
NM_001163258.1	2000	Silent Mutation	CTA,CTG	L488L	NP_001156730.1
NM_001163259.1	2000	Silent Mutation	CTA,CTG	L345L	NP_001156731.1
NM_001163260.1	2000	Silent Mutation	CTA,CTG	L298L	NP_001156732.1
NM_001319998.1	2000	Silent Mutation	CTA,CTG	L440L	NP_001306927.1
NM_018379.4	2000	Silent Mutation	CTA,CTG	L440L	NP_060849.2
XM_005245321.3	2000	Silent Mutation	CTA,CTG	L441L	XP_005245378.1
XM_005245325.3	2000	Silent Mutation	CTA,CTG	L299L	XP_005245382.1
XM_005245327.3	2000	Silent Mutation	CTA,CTG	L275L	XP_005245384.1
XM_005245328.3	2000	Silent Mutation	CTA,CTG	L274L	XP_005245385.1
XM_011509757.2	2000	Silent Mutation	CTA,CTG	L432L	XP_011508059.1
XM_011509759.2	2000	Silent Mutation	CTA,CTG	L387L	XP_011508061.1
XM_017001770.1	2000	Silent Mutation	CTA,CTG	L440L	XP_016857259.1
XM_017001771.1	2000	Silent Mutation	CTA,CTG	L440L	XP_016857260.1
XM_017001772.1	2000	Silent Mutation	CTA,CTG	L440L	XP_016857261.1
XM_017001773.1	2000	Silent Mutation	CTA,CTG	L431L	XP_016857262.1
XM_017001774.1	2000	Silent Mutation	CTA,CTG	L431L	XP_016857263.1
XM_017001775.1	2000	Silent Mutation	CTA,CTG	L387L	XP_016857264.1
XM_017001776.1	2000	Silent Mutation	CTA,CTG	L378L	XP_016857265.1
XM_017001777.1	2000	Silent Mutation	CTA,CTG	L488L	XP_016857266.1

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