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APP (exon)
QuickView for rs63750973;jsessionid=0D89EADF7072BEB6E02804F41BA302BA (snp)
-
Macaque
C
-
-
Human
C|T
- Chimp
C
-
-
Mouse
C
Rat
C
- Type:
- snp
- Organism:
- Homo sapiens
- Alleles:
- C|T
- Chromosomal Location:
- chr 21 : 26185975 (build 36.3)
- Strand:
- -
- Flanking Sequence:
- TCATAGCGA [ C | T ] AGTGATCGTCA
- Update Date:
- Jun 09 2008
- Validated:
- NO
- Associated Gene(s):
- APP
- Related URLs:
- NCBI dbSNP
APP (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000484
|
C2141T | NP_000475 | Missense | T714I |
|
NM_201413
|
C2084T | NP_958816 | Missense | T695I |
|
NM_201414
|
C1916T | NP_958817 | Missense | T639I |
