Product Details

SNP ID

rs200186614

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:88196485 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTGGATAAATACCCCAGGAATGA[A/T]TACCTAGAAAATCAAAGACACAAAT

Phenotype

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

TMEM161B PubMed Links

Gene Details

Gene

TMEM161B

Gene Name

transmembrane protein 161B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001289007.1	1296	Missense Mutation	AAT,ATT	N397I	NP_001275936.1
NM_001289008.1	1296	Missense Mutation	AAT,ATT	N386I	NP_001275937.1
NM_153354.4	1296	Intron			NP_699185.1
XM_006714553.1	1296	Intron			XP_006714616.1
XM_006714554.3	1296	Intron			XP_006714617.1
XM_006714555.3	1296	Intron			XP_006714618.1
XM_006714556.3	1296	Missense Mutation	AAT,ATT	N270I	XP_006714619.2
XM_011543201.2	1296	Intron			XP_011541503.1
XM_011543202.2	1296	Missense Mutation	AAT,ATT	N270I	XP_011541504.2
XM_011543203.2	1296	Missense Mutation	AAT,ATT	N252I	XP_011541505.2
XM_011543204.2	1296	Missense Mutation	AAT,ATT	N215I	XP_011541506.2
XM_017009093.1	1296	Missense Mutation	AAT,ATT	N397I	XP_016864582.1
XM_017009094.1	1296	Missense Mutation	AAT,ATT	N386I	XP_016864583.1
XM_017009095.1	1296	Missense Mutation	AAT,ATT	N397I	XP_016864584.1
XM_017009096.1	1296	Missense Mutation	AAT,ATT	N270I	XP_016864585.1
XM_017009097.1	1296	Missense Mutation	AAT,ATT	N270I	XP_016864586.1
XM_017009098.1	1296	Missense Mutation	AAT,ATT	N270I	XP_016864587.1
XM_017009099.1	1296	Missense Mutation	AAT,ATT	N270I	XP_016864588.1
XM_017009100.1	1296	Missense Mutation	ATC,TTC	I354F	XP_016864589.1
XM_017009101.1	1296	Missense Mutation	AAT,ATT	N215I	XP_016864590.1
XM_017009102.1	1296	Missense Mutation	AAT,ATT	N215I	XP_016864591.1
XM_017009103.1	1296	Intron			XP_016864592.1
XM_017009104.1	1296	Missense Mutation	AAT,ATT	N118I	XP_016864593.1
XM_017009105.1	1296	Intron			XP_016864594.1
XM_017009106.1	1296	Intron			XP_016864595.1
XM_017009107.1	1296	Intron			XP_016864596.1
XM_017009108.1	1296	Intron			XP_016864597.1
XM_017009109.1	1296	Missense Mutation	ATC,TTC	I238F	XP_016864598.1
XM_017009110.1	1296	Missense Mutation	ATC,TTC	I238F	XP_016864599.1

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