Product Details

SNP ID

rs199557562

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:138132625 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGTAGTTGAGTCCTGCCACCAAGA[A/G]AAACTTCTCCAGGAAGAGTTCTGAA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM135B PubMed Links

Gene Details

Gene

FAM135B

Gene Name

family with sequence similarity 135 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015912.3	5033	Missense Mutation	CTC,TTC	L1397F	NP_056996.2
XM_011517056.2	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515358.1
XM_011517058.2	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515360.1
XM_011517059.1	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515361.1
XM_011517060.2	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515362.1
XM_011517061.2	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515363.1
XM_011517062.1	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515364.1
XM_011517063.2	5033	Missense Mutation	CTC,TTC	L1401F	XP_011515365.1
XM_011517064.2	5033	Missense Mutation	CTC,TTC	L1397F	XP_011515366.1
XM_011517065.1	5033	Missense Mutation	CTC,TTC	L1385F	XP_011515367.1
XM_011517068.2	5033	Missense Mutation	CTC,TTC	L1298F	XP_011515370.1
XM_011517069.2	5033	Missense Mutation	CTC,TTC	L1279F	XP_011515371.1
XM_011517070.2	5033	Intron			XP_011515372.1
XM_011517072.2	5033	Missense Mutation	CTC,TTC	L1200F	XP_011515374.1
XM_011517073.2	5033	Missense Mutation	CTC,TTC	L1168F	XP_011515375.1
XM_011517074.1	5033	Missense Mutation	CTC,TTC	L1152F	XP_011515376.1
XM_017013470.1	5033	Missense Mutation	CTC,TTC	L1397F	XP_016868959.1
XM_017013471.1	5033	Missense Mutation	CTC,TTC	L1382F	XP_016868960.1

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