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CACCAAGTGGCTGGTCTCCAGTGAG[C/T]AGGACTTGGGGGCAGGCCTCGGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609344 | ||||||||||||||||||||
Literature Links: |
KCP 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 |
KCP - kielin/chordin-like protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135914.1 | 4879 | Silent Mutation | CTA,CTG | L,L 1482 | NP_001129386.1 | |
NM_199349.2 | 4879 | Intron | NP_955381.2 | |||
XM_017012184.1 | 4879 | Silent Mutation | CTA,CTG | L,L 1612 | XP_016867673.1 | |
XM_017012185.1 | 4879 | Silent Mutation | CTA,CTG | L,L 1607 | XP_016867674.1 | |
XM_017012186.1 | 4879 | Intron | XP_016867675.1 | |||
XM_017012187.1 | 4879 | Intron | XP_016867676.1 | |||
XM_017012188.1 | 4879 | Intron | XP_016867677.1 | |||
XM_017012189.1 | 4879 | Intron | XP_016867678.1 | |||
XM_017012190.1 | 4879 | UTR 3 | XP_016867679.1 | |||
XM_017012191.1 | 4879 | Silent Mutation | CTA,CTG | L,L 1326 | XP_016867680.1 | |
XM_017012192.1 | 4879 | Silent Mutation | CTA,CTG | L,L 1326 | XP_016867681.1 | |
XM_017012193.1 | 4879 | Intron | XP_016867682.1 | |||
XM_017012194.1 | 4879 | Intron | XP_016867683.1 |
LOC100130705 - uncharacterized LOC100130705 | ||||||
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There are no transcripts associated with this gene. |