Product Details

SNP ID

rs145948376

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:37518960 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGTTCAGAGCAGGTCAGGCAGGA[C/T]GAGGCCAGGAGGCTTTGGTTCGACA

Phenotype

MIM: 606618 MIM: 607291

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

DUSP14 PubMed Links

Gene Details

Gene

DUSP14

Gene Name

dual specificity phosphatase 14

There are no transcripts associated with this gene.

Gene

SYNRG

Gene Name

synergin, gamma

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163544.2	4132	Missense Mutation	ATC,GTC	I1231V	NP_001157016.1
NM_001163545.2	4132	Missense Mutation	ATC,GTC	I1230V	NP_001157017.1
NM_001163546.2	4132	Missense Mutation	ATC,GTC	I1174V	NP_001157018.1
NM_001163547.2	4132	Missense Mutation	ATC,GTC	I1103V	NP_001157019.1
NM_007247.5	4132	Missense Mutation	ATC,GTC	I1309V	NP_009178.3
NM_080550.4	4132	Missense Mutation	ATC,GTC	I1219V	NP_542117.3
NM_198882.2	4132	Missense Mutation	ATC,GTC	I1254V	NP_942583.1
XM_005256980.4	4132	Missense Mutation	ATC,GTC	I1410V	XP_005257037.1
XM_017024076.1	4132	Missense Mutation	ATC,GTC	I1433V	XP_016879565.1
XM_017024077.1	4132	Missense Mutation	ATC,GTC	I1432V	XP_016879566.1
XM_017024078.1	4132	Missense Mutation	ATC,GTC	I1421V	XP_016879567.1
XM_017024079.1	4132	Missense Mutation	ATC,GTC	I1412V	XP_016879568.1
XM_017024080.1	4132	Missense Mutation	ATC,GTC	I1406V	XP_016879569.1
XM_017024081.1	4132	Missense Mutation	ATC,GTC	I1405V	XP_016879570.1
XM_017024082.1	4132	Missense Mutation	ATC,GTC	I1398V	XP_016879571.1
XM_017024083.1	4132	Missense Mutation	ATC,GTC	I1388V	XP_016879572.1
XM_017024084.1	4132	Missense Mutation	ATC,GTC	I1387V	XP_016879573.1
XM_017024085.1	4132	Missense Mutation	ATC,GTC	I1377V	XP_016879574.1
XM_017024086.1	4132	Missense Mutation	ATC,GTC	I1365V	XP_016879575.1
XM_017024087.1	4132	Missense Mutation	ATC,GTC	I1364V	XP_016879576.1
XM_017024088.1	4132	Missense Mutation	ATC,GTC	I1355V	XP_016879577.1
XM_017024089.1	4132	Missense Mutation	ATC,GTC	I1353V	XP_016879578.1
XM_017024090.1	4132	Missense Mutation	ATC,GTC	I1332V	XP_016879579.1
XM_017024091.1	4132	Missense Mutation	ATC,GTC	I1331V	XP_016879580.1
XM_017024092.1	4132	Missense Mutation	ATC,GTC	I1331V	XP_016879581.1
XM_017024093.1	4132	Missense Mutation	ATC,GTC	I1297V	XP_016879582.1
XM_017024094.1	4132	Missense Mutation	ATC,GTC	I1296V	XP_016879583.1
XM_017024095.1	4132	Missense Mutation	ATC,GTC	I1288V	XP_016879584.1
XM_017024096.1	4132	Intron			XP_016879585.1
XM_017024097.1	4132	Missense Mutation	ATC,GTC	I1264V	XP_016879586.1
XM_017024098.1	4132	Missense Mutation	ATC,GTC	I1263V	XP_016879587.1
XM_017024099.1	4132	Missense Mutation	ATC,GTC	I1253V	XP_016879588.1
XM_017024100.1	4132	Missense Mutation	ATC,GTC	I1251V	XP_016879589.1
XM_017024101.1	4132	Missense Mutation	ATC,GTC	I1250V	XP_016879590.1
XM_017024102.1	4132	Missense Mutation	ATC,GTC	I1218V	XP_016879591.1
XM_017024103.1	4132	Missense Mutation	ATC,GTC	I1208V	XP_016879592.1
XM_017024104.1	4132	Missense Mutation	ATC,GTC	I1185V	XP_016879593.1
XM_017024105.1	4132	Intron			XP_016879594.1
XM_017024106.1	4132	Missense Mutation	ATC,GTC	I1186V	XP_016879595.1

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