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AAGGGGCTGTCCTCCAGGAACTCCA[A/G]GCACTGGCCCGTGAAGTTGCAACCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609603 | ||||||||||||||||||||
Literature Links: |
CRYGN 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 |
CRYGN - crystallin gamma N | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308292.1 | 960 | Intron | NP_001295221.1 | |||
NM_144727.2 | 960 | Silent Mutation | CTG,TTG | L,L 110 | NP_653328.1 | |
XM_005249952.3 | 960 | Silent Mutation | CTG,TTG | L,L 110 | XP_005250009.1 | |
XM_011515836.1 | 960 | Silent Mutation | CTG,TTG | L,L 110 | XP_011514138.1 | |
XM_011515837.2 | 960 | Silent Mutation | CTG,TTG | L,L 75 | XP_011514139.1 | |
XM_017011773.1 | 960 | UTR 3 | XP_016867262.1 |
MIR3907 - microRNA 3907 | ||||||
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There are no transcripts associated with this gene. |