Product Details

SNP ID: rs61743634
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:33667529 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCACCGCGTTGCTGGCGCTCTGCT[C/T]CACCGGCGCGTTCAGCGGGCTGGCC
Phenotype: MIM: 189971 MIM: 612478
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ACTL10 PubMed Links

Gene Details

Gene: ACTL10
Gene Name: actin like 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024675.1	1032	Missense Mutation	TCC,TTC	S11F	NP_001019846.1

Gene: C20orf144
Gene Name: chromosome 20 open reading frame 144

There are no transcripts associated with this gene.

Gene: E2F1
Gene Name: E2F transcription factor 1

There are no transcripts associated with this gene.

Gene: NECAB3
Gene Name: N-terminal EF-hand calcium binding protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031231.3	1032	Intron			NP_112508.3
NM_031232.3	1032	Intron			NP_112509.3
XM_005260510.1	1032	Intron			XP_005260567.1
XM_011528991.1	1032	Intron			XP_011527293.1
XM_011528992.2	1032	Intron			XP_011527294.1
XM_017028015.1	1032	Intron			XP_016883504.1
XM_017028016.1	1032	Intron			XP_016883505.1

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