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VWF (exon)
QuickView for rs61750597;jsessionid=C0439C28F9E1C37207CDB88602CE22D5 (snp)
-
Macaque
G
-
-
Human
G|T
- Chimp
G
-
-
Mouse
A
Rat
G
- Type:
- snp
- Organism:
- Homo sapiens
- Alleles:
- G|T
- Chromosomal Location:
- chr 12 : 5997841 (build 36.3)
- Strand:
- -
- Flanking Sequence:
- GCTGCAGAG [ G | T ] TGCTGCTCCGG
- Update Date:
- Apr 08 2008
- Validated:
- NO
- Associated Gene(s):
- VWF
- Related URLs:
- NCBI dbSNP
VWF (exon) 
| Transcript | CDS Change | Protein | Mutation Class | AA Change |
|---|---|---|---|---|
|
NM_000552
|
G5004T | NP_000543 | Missense | R1668S |
