Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAATTTCTGTGAATCTTGCTGGAAA[C/T]GATTTAGTTTCTCTGGATTATTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607766 MIM: 614552 | ||||||||||||||||||||
Literature Links: |
ACAP2 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 |
ACAP2 - ArfGAP with coiled-coil, ankyrin repeat and PH domains 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012287.5 | 2676 | Missense Mutation | CAT,CGT | H,R 770 | NP_036419.3 | |
XM_006713557.3 | 2676 | Missense Mutation | CAT,CGT | H,R 777 | XP_006713620.1 | |
XM_011512602.2 | 2676 | Missense Mutation | CAT,CGT | H,R 812 | XP_011510904.1 | |
XM_011512603.2 | 2676 | Missense Mutation | CAT,CGT | H,R 805 | XP_011510905.1 | |
XM_011512604.2 | 2676 | Missense Mutation | CAT,CGT | H,R 768 | XP_011510906.1 | |
XM_011512605.2 | 2676 | Missense Mutation | CAT,CGT | H,R 768 | XP_011510907.1 | |
XM_011512606.2 | 2676 | Missense Mutation | CAT,CGT | H,R 768 | XP_011510908.1 | |
XM_017006046.1 | 2676 | Missense Mutation | CAT,CGT | H,R 840 | XP_016861535.1 | |
XM_017006047.1 | 2676 | Missense Mutation | CAT,CGT | H,R 833 | XP_016861536.1 | |
XM_017006048.1 | 2676 | Missense Mutation | CAT,CGT | H,R 805 | XP_016861537.1 | |
XM_017006049.1 | 2676 | Missense Mutation | CAT,CGT | H,R 798 | XP_016861538.1 |
XXYLT1 - xyloside xylosyltransferase 1 | ||||||
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There are no transcripts associated with this gene. |