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CS (exon)
QuickView for rs61738833;jsessionid=D7FCA1ADD08F413A32BD8F706BF370AD (snp)
-
Macaque
G
-
-
Human
C|T
- Chimp
G
-
-
Mouse
A
Rat
A
- Type:
- snp
- Organism:
- Homo sapiens
- Alleles:
- C|T
- Chromosomal Location:
- chr 12 : 54956066 (build 36.3)
- Strand:
- +
- Flanking Sequence:
- TGAGGTACA [ C | T ] GCGCGTGAGCT
- Update Date:
- Apr 08 2008
- Validated:
- NO
- Associated Gene(s):
- CS
- Related URLs:
- NCBI dbSNP
CS (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_004077
|
C769A | NP_004068 | Missense | L257M |
|
NM_198324
|
C571A | NP_938083 | Missense | L191M |
|
NM_004077
|
C769G | NP_004068 | Missense | L257V |
|
NM_198324
|
C571G | NP_938083 | Missense | L191V |
