Product Details
- SNP ID
-
rs150929534
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:130058023 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCTCGATGAATGTGAGCTCGTCATC[A/G]TTGTCTGCCTGGCAGTCATAAATGG
- Phenotype
-
MIM: 605953
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ASAP1
PubMed Links
Gene Details
- Gene
- ASAP1
- Gene Name
- ArfGAP with SH3 domain, ankyrin repeat and PH domain 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001247996.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1075N |
NP_001234925.1 |
| NM_018482.3 |
3312 |
Silent Mutation |
AAC,AAT |
N1082N |
NP_060952.2 |
| XM_005250925.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1085N |
XP_005250982.1 |
| XM_006716563.3 |
3312 |
Silent Mutation |
AAC,AAT |
N1085N |
XP_006716626.1 |
| XM_006716564.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1078N |
XP_006716627.1 |
| XM_006716565.3 |
3312 |
Silent Mutation |
AAC,AAT |
N1029N |
XP_006716628.1 |
| XM_006716566.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1028N |
XP_006716629.1 |
| XM_011517052.2 |
3312 |
Silent Mutation |
AAC,AAT |
N1085N |
XP_011515354.1 |
| XM_011517053.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1078N |
XP_011515355.1 |
| XM_017013467.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1040N |
XP_016868956.1 |
| XM_017013468.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1026N |
XP_016868957.1 |
| XM_017013469.1 |
3312 |
Silent Mutation |
AAC,AAT |
N1025N |
XP_016868958.1 |
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