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GTCTTGTAACTTTCTTCATCAACTG[A/C]GCTACATCCAGCTTCATCTTCACTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616381 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RSRC2 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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RSRC2 - arginine and serine rich coiled-coil 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_023012.5 | 1223 | Missense Mutation | GCA,TCA | A,S 384 | NP_075388.2 | |
XM_005253601.1 | 1223 | Missense Mutation | GCA,TCA | A,S 385 | XP_005253658.1 | |
XM_005253602.2 | 1223 | Missense Mutation | GCA,TCA | A,S 337 | XP_005253659.1 | |
XM_005253604.1 | 1223 | Missense Mutation | GCA,TCA | A,S 326 | XP_005253661.1 | |
XM_011538688.1 | 1223 | Missense Mutation | GCA,TCA | A,S 355 | XP_011536990.1 | |
XM_011538689.1 | 1223 | Missense Mutation | GCA,TCA | A,S 326 | XP_011536991.1 | |
XM_017019830.1 | 1223 | Missense Mutation | GCA,TCA | A,S 354 | XP_016875319.1 | |
XM_017019831.1 | 1223 | Missense Mutation | GCA,TCA | A,S 337 | XP_016875320.1 | |
XM_017019832.1 | 1223 | Missense Mutation | GCA,TCA | A,S 153 | XP_016875321.1 | |
XM_017019833.1 | 1223 | Missense Mutation | GCA,TCA | A,S 152 | XP_016875322.1 |
ZCCHC8 - zinc finger CCHC-type containing 8 | ||||||
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There are no transcripts associated with this gene. |