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- SNP ID:
- rs6701238
- Gene
-
FAM213BLOC100996583MMEL1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 2589061 - 2589061 on Build GRCh38
- Polymorphism:
- G/A, Transition substitution
- Context Sequence [VIC/FAM]:
CTCAGGTGAGCTGGGCCTTGGGGGC[G/A]CTGCCTGCCAGCCCACGCCCTGCCC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
37 submissions
|
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Phenotype: |
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Literature Links: |
FAM213B 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
|
| FAM213B - family with sequence similarity 213 member B | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001195736.1 | Intron | NP_001182665.1 | ||||
| NM_001195737.1 | Intron | NP_001182666.1 | ||||
| NM_001195738.1 | Intron | NP_001182667.1 | ||||
| NM_001195740.1 | Intron | NP_001182669.1 | ||||
| NM_001195741.1 | Intron | NP_001182670.1 | ||||
| NM_152371.3 | Intron | NP_689584.2 | ||||
| XM_006710354.3 | Intron | XP_006710417.1 | ||||
| XM_011540664.1 | Intron | XP_011538966.1 | ||||
| XM_011540665.1 | Intron | XP_011538967.1 | ||||
| XM_011540666.1 | Intron | XP_011538968.1 | ||||
| LOC100996583 - uncharacterized LOC100996583 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| MMEL1 - membrane metallo-endopeptidase-like 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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