Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACGGCGAGGATGGACGCACAGACC[C/T]GGCCCGTGGGCTTTCGCTGCCTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602446 | ||||||||||||||||||||
Literature Links: |
GPC5 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
GPC5 - glypican 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004466.5 | 376 | Missense Mutation | CGG,TGG | R,W 6 | NP_004457.1 | |
XM_011521054.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519356.1 | |
XM_011521055.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519357.1 | |
XM_011521056.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519358.1 | |
XM_011521057.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519359.1 | |
XM_011521058.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519360.1 | |
XM_011521059.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519361.1 | |
XM_011521060.2 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_011519362.1 | |
XM_017020435.1 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_016875924.1 | |
XM_017020436.1 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_016875925.1 | |
XM_017020437.1 | 376 | Missense Mutation | CGG,TGG | R,W 6 | XP_016875926.1 |