Product Details

SNP ID

rs11962253

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:112110932 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATTAATGCATAATTTTTAGAGAGA[A/C]TGTTTCCCAGGTTGAATGCTTGACT

Phenotype

MIM: 600133

Polymorphism

A/C, Transversion 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		Intron			NP_001098676.2
NM_001105207.2		Intron			NP_001098677.2
NM_001105208.2		Intron			NP_001098678.1
NM_001105209.2		Intron			NP_001098679.1
NM_002290.4		Intron			NP_002281.3
XM_005266983.3		Intron			XP_005267040.2
XM_005266984.3		Intron			XP_005267041.2
XM_017010854.1		Intron			XP_016866343.1

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