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CCTCATCCCACATGCAAATCCGCTG[C/T]CTGTCTCTATCCTCCCACCCCTTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 126340 MIM: 607463 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ERCC2 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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ERCC2 - ERCC excision repair 2, TFIIH core complex helicase subunit | ||||||
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There are no transcripts associated with this gene. |
PPP1R13L - protein phosphatase 1 regulatory subunit 13 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142502.1 | Intron | NP_001135974.1 | ||||
NM_006663.3 | Intron | NP_006654.2 | ||||
XM_017026177.1 | Intron | XP_016881666.1 | ||||
XM_017026178.1 | Intron | XP_016881667.1 | ||||
XM_017026179.1 | Intron | XP_016881668.1 |