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SNP ID: rs138333574
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:36612159 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCAGCCCCTTGGAACTTGGAAGACC[C/T]GTGTTTCCTGGACCGCGAATCAGTG
Phenotype: MIM: 606577
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C20orf24 PubMed Links

Gene Details

Gene: C20orf24
Gene Name: chromosome 20 open reading frame 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199534.1	692	UTR 3			NP_001186463.1
NM_018840.4	692	UTR 3			NP_061328.1
NM_199483.2	692	Missense Mutation	CCG,CTG	P123L	NP_955777.1

Gene: SLA2
Gene Name: Src like adaptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032214.3	692	Intron			NP_115590.1
NM_175077.2	692	Intron			NP_778252.1
XM_017028098.1	692	Intron			XP_016883587.1

Gene: TGIF2-C20orf24
Gene Name: TGIF2-C20orf24 readthrough

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199535.1	692	UTR 3			NP_001186464.1

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