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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