Product Details

SNP ID

rs140423768

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:111661804 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAAAGTAGTCTTCCAGGAAGCTCT[C/G]CAAGTACTCAAAAGTGGGGCGTTCT

Phenotype

MIM: 137025

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FYN PubMed Links

Gene Details

Gene

FYN

Gene Name

FYN proto-oncogene, Src family tyrosine kinase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002037.5	1652	Missense Mutation	CAG,GAG	Q517E	NP_002028.1
NM_153047.3	1652	Missense Mutation	CAG,GAG	Q514E	NP_694592.1
NM_153048.3	1652	Missense Mutation	CAG,GAG	Q462E	NP_694593.1
XM_005266890.3	1652	Missense Mutation	CAG,GAG	Q514E	XP_005266947.1
XM_005266892.3	1652	Missense Mutation	CAG,GAG	Q462E	XP_005266949.1
XM_017010650.1	1652	Missense Mutation	CAG,GAG	Q517E	XP_016866139.1
XM_017010651.1	1652	Missense Mutation	CAG,GAG	Q517E	XP_016866140.1
XM_017010652.1	1652	Missense Mutation	CAG,GAG	Q517E	XP_016866141.1
XM_017010653.1	1652	Missense Mutation	CAG,GAG	Q517E	XP_016866142.1
XM_017010654.1	1652	Missense Mutation	CAG,GAG	Q517E	XP_016866143.1
XM_017010655.1	1652	Intron			XP_016866144.1

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