Product Details

SNP ID
rs77084366
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:151128144 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTTCAGGCTCCCCGTGAGGAGTC[A/G]CATTCATGTCTTGCGGTTGTCATAC
Phenotype
MIM: 608674
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SH3D19 PubMed Links

Gene Details

Gene
SH3D19
Gene Name
SH3 domain containing 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001009555.3 Intron NP_001009555.3
NM_001128923.1 Intron NP_001122395.1
NM_001128924.1 Intron NP_001122396.1
NM_001243349.1 Intron NP_001230278.1
XM_005262767.2 Intron XP_005262824.1
XM_011531646.1 Intron XP_011529948.1
XM_011531647.1 Intron XP_011529949.1
XM_011531648.1 Intron XP_011529950.1
XM_011531649.1 Intron XP_011529951.1
XM_017007778.1 Intron XP_016863267.1
XM_017007779.1 Intron XP_016863268.1
XM_017007780.1 Intron XP_016863269.1
XM_017007781.1 Intron XP_016863270.1
XM_017007782.1 Intron XP_016863271.1
XM_017007783.1 Intron XP_016863272.1

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