Product Details

SNP ID

rs149959295

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:197039385 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTCTGCCATTCATTTCTATGTT[A/C]TTAAGGGTTCTTGATAAGACAGAGT

Phenotype

MIM: 134580

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

F13B PubMed Links

Gene Details

Gene

F13B

Gene Name

coagulation factor XIII B chain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001994.2	2983	Missense Mutation	AGA,ATA	R660I	NP_001985.2
XM_011509283.2	2983	UTR 3			XP_011507585.1
XM_011509284.2	2983	UTR 3			XP_011507586.1
XM_011509286.2	2983	UTR 3			XP_011507588.1

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