Product Details

SNP ID

rs56179739

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:88196420 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATGGTAATTCAGAGTAAACAGAAT[C/T]GGACAGTAGACTATTATCCACTGGT

Phenotype

Polymorphism

C/T, Transition 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	1361	Missense Mutation	AAT,GAT	N419D	NP_001275936.1
NM_001289008.1	1361	Missense Mutation	AAT,GAT	N408D	NP_001275937.1
NM_153354.4	1361	Intron			NP_699185.1
XM_006714553.1	1361	Intron			XP_006714616.1
XM_006714554.3	1361	Intron			XP_006714617.1
XM_006714555.3	1361	Intron			XP_006714618.1
XM_006714556.3	1361	Missense Mutation	AAT,GAT	N292D	XP_006714619.2
XM_011543201.2	1361	Intron			XP_011541503.1
XM_011543202.2	1361	Missense Mutation	AAT,GAT	N292D	XP_011541504.2
XM_011543203.2	1361	Missense Mutation	AAT,GAT	N274D	XP_011541505.2
XM_011543204.2	1361	Missense Mutation	AAT,GAT	N237D	XP_011541506.2
XM_017009093.1	1361	Missense Mutation	AAT,GAT	N419D	XP_016864582.1
XM_017009094.1	1361	Missense Mutation	AAT,GAT	N408D	XP_016864583.1
XM_017009095.1	1361	Missense Mutation	AAT,GAT	N419D	XP_016864584.1
XM_017009096.1	1361	Missense Mutation	AAT,GAT	N292D	XP_016864585.1
XM_017009097.1	1361	Missense Mutation	AAT,GAT	N292D	XP_016864586.1
XM_017009098.1	1361	Missense Mutation	AAT,GAT	N292D	XP_016864587.1
XM_017009099.1	1361	Missense Mutation	AAT,GAT	N292D	XP_016864588.1
XM_017009100.1	1361	Silent Mutation	CCA,CCG	P375P	XP_016864589.1
XM_017009101.1	1361	Missense Mutation	AAT,GAT	N237D	XP_016864590.1
XM_017009102.1	1361	Missense Mutation	AAT,GAT	N237D	XP_016864591.1
XM_017009103.1	1361	Intron			XP_016864592.1
XM_017009104.1	1361	Missense Mutation	AAT,GAT	N140D	XP_016864593.1
XM_017009105.1	1361	Intron			XP_016864594.1
XM_017009106.1	1361	Intron			XP_016864595.1
XM_017009107.1	1361	Intron			XP_016864596.1
XM_017009108.1	1361	Intron			XP_016864597.1
XM_017009109.1	1361	Silent Mutation	CCA,CCG	P259P	XP_016864598.1
XM_017009110.1	1361	Silent Mutation	CCA,CCG	P259P	XP_016864599.1

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