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TACAAGGCAGCGAGGTCCGAGTGGC[A/G]GCCATTCTCAGCAGTCCCACTGTTG
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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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 | 3074 | Missense Mutation | CGC,TGC | R,C 922 | XP_005268782.1 | |
XM_011538031.1 | 3074 | Missense Mutation | CGC,TGC | R,C 1001 | XP_011536333.1 | |
XM_011538033.1 | 3074 | Missense Mutation | CGC,TGC | R,C 996 | XP_011536335.1 | |
XM_011538035.1 | 3074 | Missense Mutation | CGC,TGC | R,C 987 | XP_011536337.1 | |
XM_011538036.1 | 3074 | Missense Mutation | CGC,TGC | R,C 985 | XP_011536338.1 | |
XM_011538037.1 | 3074 | Missense Mutation | CGC,TGC | R,C 979 | XP_011536339.1 | |
XM_011538038.1 | 3074 | Missense Mutation | CGC,TGC | R,C 969 | XP_011536340.1 | |
XM_011538039.1 | 3074 | Missense Mutation | CGC,TGC | R,C 967 | XP_011536341.1 | |
XM_011538040.1 | 3074 | Missense Mutation | CGC,TGC | R,C 962 | XP_011536342.1 | |
XM_011538042.2 | 3074 | Missense Mutation | CGC,TGC | R,C 1019 | XP_011536344.1 | |
XM_017018998.1 | 3074 | Missense Mutation | CGC,TGC | R,C 993 | XP_016874487.1 | |
XM_017018999.1 | 3074 | Missense Mutation | CGC,TGC | R,C 1019 | XP_016874488.1 | |
XM_017019000.1 | 3074 | Missense Mutation | CGC,TGC | R,C 964 | XP_016874489.1 | |
XM_017019001.1 | 3074 | Missense Mutation | CGC,TGC | R,C 1011 | XP_016874490.1 | |
XM_017019002.1 | 3074 | Missense Mutation | CGC,TGC | R,C 954 | XP_016874491.1 | |
XM_017019003.1 | 3074 | Missense Mutation | CGC,TGC | R,C 946 | XP_016874492.1 | |
XM_017019004.1 | 3074 | Missense Mutation | CGC,TGC | R,C 944 | XP_016874493.1 | |
XM_017019005.1 | 3074 | Missense Mutation | CGC,TGC | R,C 988 | XP_016874494.1 | |
XM_017019006.1 | 3074 | Missense Mutation | CGC,TGC | R,C 988 | XP_016874495.1 | |
XM_017019007.1 | 3074 | Missense Mutation | CGC,TGC | R,C 988 | XP_016874496.1 | |
XM_017019008.1 | 3074 | Missense Mutation | CGC,TGC | R,C 935 | XP_016874497.1 | |
XM_017019009.1 | 3074 | Missense Mutation | CGC,TGC | R,C 930 | XP_016874498.1 | |
XM_017019010.1 | 3074 | Intron | XP_016874499.1 | |||
XM_017019011.1 | 3074 | Missense Mutation | CGC,TGC | R,C 978 | XP_016874500.1 | |
XM_017019012.1 | 3074 | Missense Mutation | CGC,TGC | R,C 924 | XP_016874501.1 | |
XM_017019013.1 | 3074 | Intron | XP_016874502.1 | |||
XM_017019014.1 | 3074 | Missense Mutation | CGC,TGC | R,C 970 | XP_016874503.1 | |
XM_017019015.1 | 3074 | Missense Mutation | CGC,TGC | R,C 958 | XP_016874504.1 | |
XM_017019016.1 | 3074 | Missense Mutation | CGC,TGC | R,C 956 | XP_016874505.1 | |
XM_017019017.1 | 3074 | Intron | XP_016874506.1 | |||
XM_017019018.1 | 3074 | Missense Mutation | CGC,TGC | R,C 954 | XP_016874507.1 | |
XM_017019019.1 | 3074 | Missense Mutation | CGC,TGC | R,C 944 | XP_016874508.1 | |
XM_017019020.1 | 3074 | Missense Mutation | CGC,TGC | R,C 892 | XP_016874509.1 | |
XM_017019021.1 | 3074 | Missense Mutation | CGC,TGC | R,C 938 | XP_016874510.1 | |
XM_017019022.1 | 3074 | Intron | XP_016874511.1 | |||
XM_017019023.1 | 3074 | Missense Mutation | CGC,TGC | R,C 938 | XP_016874512.1 | |
XM_017019024.1 | 3074 | Missense Mutation | CGC,TGC | R,C 938 | XP_016874513.1 | |
XM_017019025.1 | 3074 | Missense Mutation | CGC,TGC | R,C 934 | XP_016874514.1 | |
XM_017019026.1 | 3074 | Missense Mutation | CGC,TGC | R,C 912 | XP_016874515.1 | |
XM_017019027.1 | 3074 | Missense Mutation | CGC,TGC | R,C 904 | XP_016874516.1 | |
XM_017019028.1 | 3074 | Missense Mutation | CGC,TGC | R,C 904 | XP_016874517.1 | |
XM_017019029.1 | 3074 | Missense Mutation | CGC,TGC | R,C 884 | XP_016874518.1 | |
XM_017019030.1 | 3074 | Missense Mutation | CGC,TGC | R,C 649 | XP_016874519.1 | |
XM_017019031.1 | 3074 | Missense Mutation | CGC,TGC | R,C 617 | XP_016874520.1 | |
XM_017019032.1 | 3074 | Missense Mutation | CGC,TGC | R,C 583 | XP_016874521.1 | |
XM_017019033.1 | 3074 | Missense Mutation | CGC,TGC | R,C 583 | XP_016874522.1 |
STAC3 - SH3 and cysteine rich domain 3 | ||||||
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There are no transcripts associated with this gene. |