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HTR2B (exon)
PSMD1 (intron)
QuickView for rs61731723;jsessionid=D81AACA76F37F0993331EDF16D68DE17 (snp)
-
Macaque
A
-
-
Human
C|T
- Chimp
A
-
-
Mouse
G
Rat
G
- Type:
- snp
- Organism:
- Homo sapiens
- Alleles:
- C|T
- Chromosomal Location:
- chr 2 : 231681607 (build 36.3)
- Strand:
- +
- Flanking Sequence:
- CATGGCAGG [ C | T ] TTAATCCCATT
- Update Date:
- Apr 08 2008
- Validated:
- NO
- Associated Gene(s):
- HTR2B, PSMD1
- Related URLs:
- NCBI dbSNP
HTR2B (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000867
|
C1314A | NP_000858 | Missense | N438K |
|
NM_000867
|
C1314G | NP_000858 | Missense | N438K |
PSMD1 (intron)
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
-
|
- | - | - | - |
