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PTCH1 (exon)
QuickView for rs139942632 (snp)
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Macaque
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Human
A|G
- Chimp
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Mouse
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Rat
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- Type:
- SNP
- Organism:
- Homo sapiens
- Alleles:
- A|G
- Chromosomal Location:
- chr 9 : 97249104 (build 36.3)
- Strand:
- +
- Update Date:
- Nov 14 2011
- Associated Gene(s):
- PTCH1
- Related URLs:
- NCBI dbSNP
PTCH1 (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000264
|
C4255T | NP_000255 | Missense | R1419W |
|
NM_001083602
|
C4057T | NP_001077071 | Missense | R1353W |
|
NM_001083603
|
C4252T | NP_001077072 | Missense | R1418W |
|
NM_001083604
|
C3802T | NP_001077073 | Missense | R1268W |
|
NM_001083605
|
C3802T | NP_001077074 | Missense | R1268W |
|
NM_001083606
|
C3802T | NP_001077075 | Missense | R1268W |
|
NM_001083607
|
C3802T | NP_001077076 | Missense | R1268W |
