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HTR7 (exon)
QuickView for rs61732493;jsessionid=35DFFADD7678DE7A28C12FC0CA838CF6 (snp)
-
Macaque
A
-
-
Human
C|T
- Chimp
G
-
-
Mouse
G
Rat
A
- Type:
- snp
- Organism:
- Homo sapiens
- Alleles:
- C|T
- Chromosomal Location:
- chr 10 : 92498623 (build 36.3)
- Strand:
- +
- Flanking Sequence:
- CAGGGCTTC [ C | T ] TGCATGCCTGC
- Update Date:
- Apr 08 2008
- Validated:
- NO
- Associated Gene(s):
- HTR7
- Related URLs:
- NCBI dbSNP
HTR7 (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000872
|
T1248A | NP_000863 | Missense | H416Q |
|
NM_019859
|
T1248A | NP_062873 | Missense | H416Q |
|
NM_019860
|
T1248A | NP_062874 | Missense | H416Q |
|
NM_000872
|
T1248G | NP_000863 | Missense | H416Q |
|
NM_019859
|
T1248G | NP_062873 | Missense | H416Q |
|
NM_019860
|
T1248G | NP_062874 | Missense | H416Q |
