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Search Thermo Fisher Scientific
AGGATAGCCAGGGTCCGGGGCAGGC[C/T]GGCGGGCACTGTGGTCAGCTGGTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610055 | ||||||||||||||||||||
Literature Links: |
CC2D1A 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 |
CC2D1A - coiled-coil and C2 domain containing 1A | ||||||
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There are no transcripts associated with this gene. |
PODNL1 - podocan like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146254.1 | 958 | Missense Mutation | AGC,GGC | S,G 282 | NP_001139726.1 | |
NM_001146255.1 | 958 | Missense Mutation | AGC,GGC | S,G 193 | NP_001139727.1 | |
NM_024825.3 | 958 | Missense Mutation | AGC,GGC | S,G 284 | NP_079101.3 | |
XM_006722901.1 | 958 | Missense Mutation | AGC,GGC | S,G 284 | XP_006722964.1 | |
XM_006722902.1 | 958 | Missense Mutation | AGC,GGC | S,G 239 | XP_006722965.1 | |
XM_006722903.1 | 958 | Missense Mutation | AGC,GGC | S,G 195 | XP_006722966.1 | |
XM_011528308.1 | 958 | Missense Mutation | AGC,GGC | S,G 282 | XP_011526610.1 | |
XM_011528309.2 | 958 | Missense Mutation | AGC,GGC | S,G 266 | XP_011526611.1 | |
XM_011528310.2 | 958 | Missense Mutation | AGC,GGC | S,G 254 | XP_011526612.1 | |
XM_011528311.1 | 958 | Missense Mutation | AGC,GGC | S,G 251 | XP_011526613.1 | |
XM_011528313.1 | 958 | Missense Mutation | AGC,GGC | S,G 202 | XP_011526615.1 | |
XM_011528314.1 | 958 | Missense Mutation | AGC,GGC | S,G 187 | XP_011526616.1 | |
XM_011528316.1 | 958 | Missense Mutation | AGC,GGC | S,G 113 | XP_011526618.1 | |
XM_017027313.1 | 958 | Missense Mutation | AGC,GGC | S,G 187 | XP_016882802.1 |