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- SNP ID:
- rs11575897
- Gene
-
SRY - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.Y: 2787139 - 2787139 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
ACAACCTGTTGTCCAGTTGCACTTC[A/G]CTGCAGAGTACCGAAGCGGGATCTG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 480000
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Literature Links: |
SRY 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
|
| SRY - sex determining region Y | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_003140.2 | 603 | Silent Mutation | AGC,AGT | S,S 155 | NP_003131.1 | |
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