Product Details

SNP ID

rs199893965

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:17135370 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAGAGGAGGCGATGGTGACCCGGA[C/T]GCAGCTGCTGGAGGAAGAGCTGAGC

Phenotype

MIM: 611870

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CNTLN PubMed Links

Gene Details

Gene

CNTLN

Gene Name

centlein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001114395.2	380	Missense Mutation	ACG,ATG	T102M	NP_001107867.1
NM_001286984.1	380	Missense Mutation	ACG,ATG	T102M	NP_001273913.1
NM_001286985.1	380	Intron			NP_001273914.1
NM_017738.3	380	Missense Mutation	ACG,ATG	T102M	NP_060208.2
XM_005251492.1	380	Missense Mutation	ACG,ATG	T102M	XP_005251549.1
XM_006716793.3	380	Intron			XP_006716856.1
XM_011517941.2	380	Missense Mutation	ACG,ATG	T102M	XP_011516243.1
XM_017014839.1	380	Missense Mutation	ACG,ATG	T102M	XP_016870328.1
XM_017014840.1	380	Missense Mutation	ACG,ATG	T102M	XP_016870329.1
XM_017014841.1	380	Missense Mutation	ACG,ATG	T102M	XP_016870330.1
XM_017014842.1	380	Missense Mutation	ACG,ATG	T102M	XP_016870331.1
XM_017014843.1	380	Missense Mutation	ACG,ATG	T102M	XP_016870332.1
XM_017014844.1	380	Intron			XP_016870333.1
XM_017014845.1	380	Intron			XP_016870334.1
XM_017014846.1	380	Intron			XP_016870335.1
XM_017014847.1	380	Intron			XP_016870336.1

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