Product Details
- SNP ID
-
rs199556436
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:50445357 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCGCACAGTTCTAAAAGCATTTTCA[A/G]AATCAATGTAAGCTATGGGTCGAAC
- Phenotype
-
MIM: 615383
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FIGNL1
PubMed Links
Gene Details
- Gene
- FIGNL1
- Gene Name
- fidgetin like 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001042762.2 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_001036227.1 |
NM_001287492.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_001274421.1 |
NM_001287493.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_001274422.1 |
NM_001287494.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_001274423.1 |
NM_001287495.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_001274424.1 |
NM_001287496.1 |
2310 |
Missense Mutation |
TCT,TTT |
S533F |
NP_001274425.1 |
NM_022116.4 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
NP_071399.2 |
XM_011515470.2 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
XP_011513772.1 |
XM_017012501.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
XP_016867990.1 |
XM_017012502.1 |
2310 |
Missense Mutation |
TCT,TTT |
S644F |
XP_016867991.1 |
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