Product Details

SNP ID
rs142970959
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:65581040 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGGCTGACTCTGCCCTTCTCCC[C/G]TCTCCTACCATTCCCAGATCCCTCT
Phenotype
MIM: 616128 MIM: 606044
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
EHBP1L1 PubMed Links

Gene Details

Gene
EHBP1L1
Gene Name
EH domain binding protein 1 like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099409.1 Intron NP_001092879.1
XM_005273867.3 Intron XP_005273924.1
XM_005273868.3 Intron XP_005273925.1
XM_005273869.3 Intron XP_005273926.1
XM_005273870.3 Intron XP_005273927.1
XM_006718486.3 Intron XP_006718549.1
XM_006718487.3 Intron XP_006718550.1
XM_011544886.2 Intron XP_011543188.1
XM_017017467.1 Intron XP_016872956.1
XM_017017468.1 Intron XP_016872957.1
XM_017017469.1 Intron XP_016872958.1
Gene
FAM89B
Gene Name
family with sequence similarity 89 member B
There are no transcripts associated with this gene.

Gene
SSSCA1
Gene Name
Sjogren syndrome/scleroderma autoantigen 1
There are no transcripts associated with this gene.

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