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TCTCAGCAGTCCCACTGTTGTCCCC[A/C]CCACCCCCTCCAGGCAGCCCCTGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615521 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
R3HDM2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
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R3HDM2 - R3H domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005268725.3 | 3043 | Silent Mutation | GGG,GGT | G,G 911 | XP_005268782.1 | |
XM_011538031.1 | 3043 | Silent Mutation | GGG,GGT | G,G 990 | XP_011536333.1 | |
XM_011538033.1 | 3043 | Silent Mutation | GGG,GGT | G,G 985 | XP_011536335.1 | |
XM_011538035.1 | 3043 | Silent Mutation | GGG,GGT | G,G 976 | XP_011536337.1 | |
XM_011538036.1 | 3043 | Silent Mutation | GGG,GGT | G,G 974 | XP_011536338.1 | |
XM_011538037.1 | 3043 | Silent Mutation | GGG,GGT | G,G 968 | XP_011536339.1 | |
XM_011538038.1 | 3043 | Silent Mutation | GGG,GGT | G,G 958 | XP_011536340.1 | |
XM_011538039.1 | 3043 | Silent Mutation | GGG,GGT | G,G 956 | XP_011536341.1 | |
XM_011538040.1 | 3043 | Silent Mutation | GGG,GGT | G,G 951 | XP_011536342.1 | |
XM_011538042.2 | 3043 | Silent Mutation | GGG,GGT | G,G 1008 | XP_011536344.1 | |
XM_017018998.1 | 3043 | Silent Mutation | GGG,GGT | G,G 982 | XP_016874487.1 | |
XM_017018999.1 | 3043 | Silent Mutation | GGG,GGT | G,G 1008 | XP_016874488.1 | |
XM_017019000.1 | 3043 | Silent Mutation | GGG,GGT | G,G 953 | XP_016874489.1 | |
XM_017019001.1 | 3043 | Silent Mutation | GGG,GGT | G,G 1000 | XP_016874490.1 | |
XM_017019002.1 | 3043 | Silent Mutation | GGG,GGT | G,G 943 | XP_016874491.1 | |
XM_017019003.1 | 3043 | Silent Mutation | GGG,GGT | G,G 935 | XP_016874492.1 | |
XM_017019004.1 | 3043 | Silent Mutation | GGG,GGT | G,G 933 | XP_016874493.1 | |
XM_017019005.1 | 3043 | Silent Mutation | GGG,GGT | G,G 977 | XP_016874494.1 | |
XM_017019006.1 | 3043 | Silent Mutation | GGG,GGT | G,G 977 | XP_016874495.1 | |
XM_017019007.1 | 3043 | Silent Mutation | GGG,GGT | G,G 977 | XP_016874496.1 | |
XM_017019008.1 | 3043 | Silent Mutation | GGG,GGT | G,G 924 | XP_016874497.1 | |
XM_017019009.1 | 3043 | Silent Mutation | GGG,GGT | G,G 919 | XP_016874498.1 | |
XM_017019010.1 | 3043 | Intron | XP_016874499.1 | |||
XM_017019011.1 | 3043 | Silent Mutation | GGG,GGT | G,G 967 | XP_016874500.1 | |
XM_017019012.1 | 3043 | Silent Mutation | GGG,GGT | G,G 913 | XP_016874501.1 | |
XM_017019013.1 | 3043 | Intron | XP_016874502.1 | |||
XM_017019014.1 | 3043 | Silent Mutation | GGG,GGT | G,G 959 | XP_016874503.1 | |
XM_017019015.1 | 3043 | Silent Mutation | GGG,GGT | G,G 947 | XP_016874504.1 | |
XM_017019016.1 | 3043 | Silent Mutation | GGG,GGT | G,G 945 | XP_016874505.1 | |
XM_017019017.1 | 3043 | Intron | XP_016874506.1 | |||
XM_017019018.1 | 3043 | Silent Mutation | GGG,GGT | G,G 943 | XP_016874507.1 | |
XM_017019019.1 | 3043 | Silent Mutation | GGG,GGT | G,G 933 | XP_016874508.1 | |
XM_017019020.1 | 3043 | Silent Mutation | GGG,GGT | G,G 881 | XP_016874509.1 | |
XM_017019021.1 | 3043 | Silent Mutation | GGG,GGT | G,G 927 | XP_016874510.1 | |
XM_017019022.1 | 3043 | Intron | XP_016874511.1 | |||
XM_017019023.1 | 3043 | Silent Mutation | GGG,GGT | G,G 927 | XP_016874512.1 | |
XM_017019024.1 | 3043 | Silent Mutation | GGG,GGT | G,G 927 | XP_016874513.1 | |
XM_017019025.1 | 3043 | Silent Mutation | GGG,GGT | G,G 923 | XP_016874514.1 | |
XM_017019026.1 | 3043 | Silent Mutation | GGG,GGT | G,G 901 | XP_016874515.1 | |
XM_017019027.1 | 3043 | Silent Mutation | GGG,GGT | G,G 893 | XP_016874516.1 | |
XM_017019028.1 | 3043 | Silent Mutation | GGG,GGT | G,G 893 | XP_016874517.1 | |
XM_017019029.1 | 3043 | Silent Mutation | GGG,GGT | G,G 873 | XP_016874518.1 | |
XM_017019030.1 | 3043 | Silent Mutation | GGG,GGT | G,G 638 | XP_016874519.1 | |
XM_017019031.1 | 3043 | Silent Mutation | GGG,GGT | G,G 606 | XP_016874520.1 | |
XM_017019032.1 | 3043 | Silent Mutation | GGG,GGT | G,G 572 | XP_016874521.1 | |
XM_017019033.1 | 3043 | Silent Mutation | GGG,GGT | G,G 572 | XP_016874522.1 |
STAC3 - SH3 and cysteine rich domain 3 | ||||||
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There are no transcripts associated with this gene. |