Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAGCCCATGCTGAAGCCAGCCCCT[C/G]CTGCCCCAGCATTGGTGCTGCTGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608246 | ||||||||||||||||||||
Literature Links: |
KRT72 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 |
KRT72 - keratin 72 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146225.1 | 1164 | Missense Mutation | GCA,GGA | A,G 459 | NP_001139697.1 | |
NM_001146226.1 | 1164 | Missense Mutation | GCA,GGA | A,G 417 | NP_001139698.1 | |
NM_080747.2 | 1164 | Missense Mutation | GCA,GGA | A,G 459 | NP_542785.1 | |
XM_017018833.1 | 1164 | Missense Mutation | GCA,GGA | A,G 393 | XP_016874322.1 | |
XM_017018834.1 | 1164 | Missense Mutation | GCA,GGA | A,G 390 | XP_016874323.1 | |
XM_017018835.1 | 1164 | Missense Mutation | GCA,GGA | A,G 387 | XP_016874324.1 | |
XM_017018836.1 | 1164 | Missense Mutation | GCA,GGA | A,G 367 | XP_016874325.1 | |
XM_017018837.1 | 1164 | Missense Mutation | GCA,GGA | A,G 219 | XP_016874326.1 |