Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACAGATGGCAGTGGCTGCGGTGGGG[A/G]GCGGGCTGGGCAGGAAGCGGGCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601964 MIM: 604497 | ||||||||||||||||||||
Literature Links: |
DNAJC7 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 |
DNAJC7 - DnaJ heat shock protein family (Hsp40) member C7 | ||||||
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There are no transcripts associated with this gene. |
NKIRAS2 - NFKB inhibitor interacting Ras like 2 | ||||||
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There are no transcripts associated with this gene. |
ZNF385C - zinc finger protein 385C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242704.1 | 2033 | Missense Mutation | CCC,CTC | P,L 368 | NP_001229633.1 | |
XM_006721751.3 | 2033 | Missense Mutation | CCC,CTC | P,L 315 | XP_006721814.1 | |
XM_011524475.2 | 2033 | Intron | XP_011522777.1 | |||
XM_011524476.1 | 2033 | Intron | XP_011522778.1 | |||
XM_011524477.2 | 2033 | Intron | XP_011522779.1 | |||
XM_011524478.2 | 2033 | Intron | XP_011522780.1 | |||
XM_011524479.2 | 2033 | Missense Mutation | CCC,CTC | P,L 448 | XP_011522781.1 | |
XM_011524482.2 | 2033 | Missense Mutation | CCC,CTC | P,L 447 | XP_011522784.1 | |
XM_011524483.2 | 2033 | Missense Mutation | CCC,CTC | P,L 443 | XP_011522785.1 | |
XM_017024314.1 | 2033 | Missense Mutation | CCC,CTC | P,L 490 | XP_016879803.1 | |
XM_017024315.1 | 2033 | Missense Mutation | CCC,CTC | P,L 490 | XP_016879804.1 | |
XM_017024316.1 | 2033 | Missense Mutation | CCC,CTC | P,L 489 | XP_016879805.1 | |
XM_017024317.1 | 2033 | Missense Mutation | CCC,CTC | P,L 485 | XP_016879806.1 | |
XM_017024318.1 | 2033 | Missense Mutation | CCC,CTC | P,L 484 | XP_016879807.1 | |
XM_017024319.1 | 2033 | Missense Mutation | CCC,CTC | P,L 442 | XP_016879808.1 | |
XM_017024320.1 | 2033 | Missense Mutation | CCC,CTC | P,L 357 | XP_016879809.1 | |
XM_017024321.1 | 2033 | Intron | XP_016879810.1 |