Product Details

SNP ID

rs61781203

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:32221921 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTAGCAACTGCTGGGCCCAGGT[A/C]GGCTCATGAACCCGCTGCAGGCCGG

Phenotype

MIM: 603911

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

DCDC2B PubMed Links

Gene Details

Gene

DCDC2B

Gene Name

doublecortin domain containing 2B

There are no transcripts associated with this gene.

Gene

EIF3I

Gene Name

eukaryotic translation initiation factor 3 subunit I

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003757.3	145	UTR 5			NP_003748.1
XM_017002671.1	145	Intron			XP_016858160.1

Gene

MTMR9LP

Gene Name

myotubularin related protein 9-like, pseudogene

There are no transcripts associated with this gene.

Gene

TMEM234

Gene Name

transmembrane protein 234

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019118.4	145	Silent Mutation			NP_061991.3
XM_011541795.2	145	Silent Mutation			XP_011540097.1
XM_017001812.1	145	Silent Mutation			XP_016857301.1
XM_017001813.1	145	Silent Mutation			XP_016857302.1
XM_017001814.1	145	Silent Mutation			XP_016857303.1
XM_017001815.1	145	Silent Mutation			XP_016857304.1
XM_017001816.1	145	Silent Mutation			XP_016857305.1
XM_017001817.1	145	Silent Mutation			XP_016857306.1
XM_017001818.1	145	Silent Mutation			XP_016857307.1
XM_017001819.1	145	Silent Mutation			XP_016857308.1
XM_017001820.1	145	Silent Mutation			XP_016857309.1
XM_017001821.1	145	Silent Mutation			XP_016857310.1
XM_017001822.1	145	Silent Mutation			XP_016857311.1
XM_017001823.1	145	Silent Mutation			XP_016857312.1
XM_017001824.1	145	Silent Mutation			XP_016857313.1
XM_017001825.1	145	Silent Mutation			XP_016857314.1
XM_017001826.1	145	Silent Mutation			XP_016857315.1
XM_017001827.1	145	Silent Mutation			XP_016857316.1
XM_017001828.1	145	Silent Mutation			XP_016857317.1
XM_017001829.1	145	Silent Mutation			XP_016857318.1
XM_017001830.1	145	Silent Mutation			XP_016857319.1
XM_017001831.1	145	Intron			XP_016857320.1

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