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- SNP ID:
- rs78849401
- Gene
-
NEMP1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 57071931 - 57071931 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
AACAACTACGACATTTCTGAAAGGA[C/T]CTATTTTGTACAATCACTGTTACAG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616496
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Literature Links: |
NEMP1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| NEMP1 - nuclear envelope integral membrane protein 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001130963.1 | Intron | NP_001124435.1 | ||||
| NM_015257.2 | Intron | NP_056072.2 | ||||
| XM_011538056.2 | Intron | XP_011536358.1 | ||||
| XM_011538057.2 | Intron | XP_011536359.1 | ||||
| XM_011538058.2 | Intron | XP_011536360.1 | ||||
| XM_011538059.1 | Intron | XP_011536361.1 | ||||
| XM_011538060.2 | Intron | XP_011536362.1 | ||||
| XM_017019077.1 | Intron | XP_016874566.1 | ||||
| XM_017019078.1 | Intron | XP_016874567.1 | ||||
| XM_017019079.1 | Intron | XP_016874568.1 | ||||
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