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CTCTAGGGTGAAGGCCATGCCGCCT[C/T]CTGGGAAAGTTCCCCGAAAGGAGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607099 | ||||||||||||||||||||
Literature Links: |
C2CD2L 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 |
C2CD2L - C2CD2 like | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HINFP - histone H4 transcription factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243259.1 | 192 | Missense Mutation | CCT,TCT | P,S 4 | NP_001230188.1 | |
NM_015517.4 | 192 | Missense Mutation | CCT,TCT | P,S 4 | NP_056332.2 | |
NM_198971.2 | 192 | Missense Mutation | CCT,TCT | P,S 4 | NP_945322.1 | |
XM_011542744.2 | 192 | Missense Mutation | CCT,TCT | P,S 18 | XP_011541046.1 | |
XM_011542745.2 | 192 | Missense Mutation | CCT,TCT | P,S 4 | XP_011541047.1 | |
XM_011542746.1 | 192 | Intron | XP_011541048.1 | |||
XM_017017499.1 | 192 | Missense Mutation | CCT,TCT | P,S 18 | XP_016872988.1 | |
XM_017017500.1 | 192 | Missense Mutation | CCT,TCT | P,S 4 | XP_016872989.1 | |
XM_017017501.1 | 192 | Missense Mutation | CCT,TCT | P,S 4 | XP_016872990.1 | |
XM_017017502.1 | 192 | UTR 5 | XP_016872991.1 | |||
XM_017017503.1 | 192 | UTR 5 | XP_016872992.1 | |||
XM_017017504.1 | 192 | UTR 5 | XP_016872993.1 | |||
XM_017017505.1 | 192 | UTR 5 | XP_016872994.1 | |||
XM_017017506.1 | 192 | UTR 5 | XP_016872995.1 | |||
XM_017017507.1 | 192 | UTR 5 | XP_016872996.1 | |||
XM_017017508.1 | 192 | UTR 5 | XP_016872997.1 | |||
XM_017017509.1 | 192 | Intron | XP_016872998.1 |