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SNP ID: rs143464338
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:138946380 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGCTCGCCGCCGCCCTCGCGCGGCA[C/T]CTTGATGAAGCACTCGTTGAGGCTG
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	761	Missense Mutation	ATG,GTG	M115V	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	761	Intron			NP_001035150.1
XM_005247443.3	761	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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