Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTGGCTTCGGAGGCAGAGGCGAA[A/G]GCTGAGCAGAGAAGTTCAGGATGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 608317 MIM: 615826 | ||||||||||||||||||||
Literature Links: |
GRHL3 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 |
GRHL3 - grainyhead like transcription factor 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195010.1 | 1156 | Intron | NP_001181939.1 | |||
NM_021180.3 | 1156 | Intron | NP_067003.2 | |||
NM_198173.2 | 1156 | Intron | NP_937816.1 | |||
NM_198174.2 | 1156 | Intron | NP_937817.3 | |||
XM_011541869.1 | 1156 | Intron | XP_011540171.1 | |||
XM_011541870.2 | 1156 | Intron | XP_011540172.1 |
STPG1 - sperm tail PG-rich repeat containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199012.1 | 1156 | Missense Mutation | CCT,CTT | P,L 257 | NP_001185941.1 | |
NM_001199013.1 | 1156 | Missense Mutation | CCT,CTT | P,L 257 | NP_001185942.1 | |
NM_001199014.1 | 1156 | Missense Mutation | CCT,CTT | P,L 165 | NP_001185943.1 | |
NM_178122.4 | 1156 | Missense Mutation | CCT,CTT | P,L 210 | NP_835223.1 | |
XM_006711025.2 | 1156 | Missense Mutation | CCT,CTT | P,L 257 | XP_006711088.1 | |
XM_011542403.2 | 1156 | Missense Mutation | CCT,CTT | P,L 289 | XP_011540705.1 | |
XM_011542404.1 | 1156 | Missense Mutation | CCT,CTT | P,L 257 | XP_011540706.1 | |
XM_017002768.1 | 1156 | Missense Mutation | CCT,CTT | P,L 210 | XP_016858257.1 | |
XM_017002769.1 | 1156 | Missense Mutation | CCT,CTT | P,L 165 | XP_016858258.1 | |
XM_017002770.1 | 1156 | Missense Mutation | CCT,CTT | P,L 165 | XP_016858259.1 |