Product Details

SNP ID
rs145897390
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:112109565 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGAAGGGTTTGCTGGGGGCCAAGC[A/G]TGGTGTCAGTAGAGATTCTGAAAAG
Phenotype
MIM: 600133
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM229B PubMed Links

Gene Details

Gene
FAM229B
Gene Name
family with sequence similarity 229 member B
There are no transcripts associated with this gene.

Gene
LAMA4
Gene Name
laminin subunit alpha 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001105206.2 5738 Missense Mutation NP_001098676.2
NM_001105207.2 5738 Missense Mutation NP_001098677.2
NM_001105208.2 5738 Intron NP_001098678.1
NM_001105209.2 5738 Intron NP_001098679.1
NM_002290.4 5738 Missense Mutation NP_002281.3
XM_005266983.3 5738 Missense Mutation XP_005267040.2
XM_005266984.3 5738 Missense Mutation XP_005267041.2
XM_017010854.1 5738 Missense Mutation XP_016866343.1

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