Product Details
- SNP ID
-
rs139179940
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:110101793 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAGCTGTAACTGTGACAGGTGATGA[C/T]GGTCGAATGCCAGGTGGAGGCAGAG
- Phenotype
-
MIM: 605035
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
WASF1
PubMed Links
Gene Details
- Gene
- WASF1
- Gene Name
- WAS protein family member 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001024934.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
NP_001020105.1 |
NM_001024935.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
NP_001020106.1 |
NM_001024936.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
NP_001020107.1 |
NM_003931.2 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
NP_003922.1 |
XM_005267203.3 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_005267260.1 |
XM_005267205.2 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_005267262.1 |
XM_005267206.2 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_005267263.1 |
XM_005267207.2 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_005267264.1 |
XM_011536233.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_011534535.1 |
XM_011536234.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_011534536.1 |
XM_011536235.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_011534537.1 |
XM_017011437.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_016866926.1 |
XM_017011438.1 |
1511 |
Silent Mutation |
CCA,CCG |
P439P |
XP_016866927.1 |
XM_017011439.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866928.1 |
XM_017011440.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866929.1 |
XM_017011441.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866930.1 |
XM_017011442.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866931.1 |
XM_017011443.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866932.1 |
XM_017011444.1 |
1511 |
Silent Mutation |
CCA,CCG |
P438P |
XP_016866933.1 |
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