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AAGTGATTCTCCTGCCATGGCCTCA[A/G]TATCAAATTTGCATTTTTTTCCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608674 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SH3D19 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
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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SH3D19 - SH3 domain containing 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009555.3 | Intron | NP_001009555.3 | ||||
NM_001128923.1 | Intron | NP_001122395.1 | ||||
NM_001128924.1 | Intron | NP_001122396.1 | ||||
NM_001243349.1 | Intron | NP_001230278.1 | ||||
XM_005262767.2 | Intron | XP_005262824.1 | ||||
XM_011531646.1 | Intron | XP_011529948.1 | ||||
XM_011531647.1 | Intron | XP_011529949.1 | ||||
XM_011531648.1 | Intron | XP_011529950.1 | ||||
XM_011531649.1 | Intron | XP_011529951.1 | ||||
XM_017007778.1 | Intron | XP_016863267.1 | ||||
XM_017007779.1 | Intron | XP_016863268.1 | ||||
XM_017007780.1 | Intron | XP_016863269.1 | ||||
XM_017007781.1 | Intron | XP_016863270.1 | ||||
XM_017007782.1 | Intron | XP_016863271.1 | ||||
XM_017007783.1 | Intron | XP_016863272.1 |