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SNP ID: rs200719486
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:138946369 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTTGCCCTTGCGCTCGCCGCCGCC[C/T]TCGCGCGGCACCTTGATGAAGCACT
Phenotype: MIM: 605597
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: FOXL2 PubMed Links

Gene Details

Gene: FOXL2
Gene Name: forkhead box L2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023067.3	772	Silent Mutation	GAA,GAG	E118E	NP_075555.1

Gene: FOXL2NB
Gene Name: FOXL2 neighbor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040061.2	772	Intron			NP_001035150.1
XM_005247443.3	772	Intron			XP_005247500.1

Gene: LINC01391
Gene Name: long intergenic non-protein coding RNA 1391

There are no transcripts associated with this gene.

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