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TTCACTACATTACAGCTGTAACAGG[A/G]TTCTTAGAGATTATATGAGAAAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
45 submissions
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Phenotype: |
MIM: 602426 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101927164 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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LOC101927164 - uncharacterized LOC101927164 | ||||||
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There are no transcripts associated with this gene. |
NVL - nuclear VCP-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243146.1 | Intron | NP_001230075.1 | ||||
NM_001243147.1 | Intron | NP_001230076.1 | ||||
NM_002533.3 | Intron | NP_002524.2 | ||||
NM_206840.2 | Intron | NP_996671.1 | ||||
XM_011544196.1 | Intron | XP_011542498.1 | ||||
XM_011544198.1 | Intron | XP_011542500.1 | ||||
XM_011544199.1 | Intron | XP_011542501.1 | ||||
XM_011544200.1 | Intron | XP_011542502.1 | ||||
XM_017001378.1 | Intron | XP_016856867.1 | ||||
XM_017001379.1 | Intron | XP_016856868.1 | ||||
XM_017001380.1 | Intron | XP_016856869.1 | ||||
XM_017001381.1 | Intron | XP_016856870.1 | ||||
XM_017001382.1 | Intron | XP_016856871.1 | ||||
XM_017001383.1 | Intron | XP_016856872.1 | ||||
XM_017001384.1 | Intron | XP_016856873.1 | ||||
XM_017001385.1 | Intron | XP_016856874.1 | ||||
XM_017001386.1 | Intron | XP_016856875.1 |