Search Thermo Fisher Scientific
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AGGGGGATGATATACTCTCCACCTG[C/T]GAGCGATGATAGGATCAGGATGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610812 MIM: 604632 | ||||||||||||||||||||
Literature Links: |
HYDIN 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 |
HYDIN - HYDIN, axonemal central pair apparatus protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198542.1 | 15238 | Intron | NP_001185471.1 | |||
NM_001198543.1 | 15238 | Intron | NP_001185472.1 | |||
NM_001270974.2 | 15238 | Missense Mutation | NP_001257903.1 | |||
NM_017558.4 | 15238 | Intron | NP_060028.2 | |||
XM_006721206.2 | 15238 | Missense Mutation | XP_006721269.1 | |||
XM_011523146.2 | 15238 | Missense Mutation | XP_011521448.1 | |||
XM_011523147.1 | 15238 | Missense Mutation | XP_011521449.1 | |||
XM_011523148.1 | 15238 | Missense Mutation | XP_011521450.1 | |||
XM_011523151.1 | 15238 | Missense Mutation | XP_011521453.1 | |||
XM_011523152.1 | 15238 | Missense Mutation | XP_011521454.1 | |||
XM_011523155.2 | 15238 | Missense Mutation | XP_011521457.1 | |||
XM_017023346.1 | 15238 | Missense Mutation | XP_016878835.1 | |||
XM_017023347.1 | 15238 | Missense Mutation | XP_016878836.1 | |||
XM_017023348.1 | 15238 | Missense Mutation | XP_016878837.1 |
VAC14 - Vac14, PIKFYVE complex component | ||||||
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There are no transcripts associated with this gene. |