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Search Thermo Fisher Scientific
AAGGCCCTTATCTATTTCTTCTTCC[A/G]TTCTTGGGAGCAGCGTGGGCAAAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608352 MIM: 608524 | ||||||||||||||||||||
Literature Links: |
ACRBP 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 |
ACRBP - acrosin binding protein | ||||||
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There are no transcripts associated with this gene. |
ING4 - inhibitor of growth family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127582.1 | 774 | Missense Mutation | CGG,TGG | R,W 246 | NP_001121054.1 | |
NM_001127583.1 | 774 | Missense Mutation | CGG,TGG | R,W 243 | NP_001121055.1 | |
NM_001127584.1 | 774 | Missense Mutation | CGG,TGG | R,W 242 | NP_001121056.1 | |
NM_001127585.1 | 774 | Missense Mutation | CGG,TGG | R,W 222 | NP_001121057.1 | |
NM_001127586.1 | 774 | UTR 3 | NP_001121058.1 | |||
NM_016162.3 | 774 | Missense Mutation | CGG,TGG | R,W 245 | NP_057246.2 | |
XM_005253698.3 | 774 | Missense Mutation | CGG,TGG | R,W 197 | XP_005253755.1 | |
XM_011520964.2 | 774 | Missense Mutation | CGG,TGG | R,W 221 | XP_011519266.1 | |
XM_011520965.2 | 774 | Missense Mutation | CGG,TGG | R,W 219 | XP_011519267.1 | |
XM_017019392.1 | 774 | Missense Mutation | CGG,TGG | R,W 196 | XP_016874881.1 | |
XM_017019393.1 | 774 | Missense Mutation | CGG,TGG | R,W 193 | XP_016874882.1 |