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TCTAATTCTCGCTTTCCAGTTAAAC[C/G]ACAGTCCATGTTAGAATTGCTTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 604950 MIM: 615858 | ||||||||||||||||||||
Literature Links: |
PHTF1 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 |
PHTF1 - putative homeodomain transcription factor 1 | ||||||
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There are no transcripts associated with this gene. |
RSBN1 - round spermatid basic protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018364.4 | 2231 | Missense Mutation | CGT,GGT | R,G 723 | NP_060834.2 | |
XM_017001518.1 | 2231 | Intron | XP_016857007.1 |