Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGCTGAGAAAGGTCCACATTGAAA[A/G]ATGACAACTTTGAATGTTCATAGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612675 | ||||||||||||||||||||
Literature Links: |
FSD2 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 |
FSD2 - fibronectin type III and SPRY domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007122.3 | 2288 | Missense Mutation | TCT,TTT | S,F 702 | NP_001007123.1 | |
NM_001281805.1 | 2288 | Missense Mutation | TCT,TTT | S,F 657 | NP_001268734.1 | |
NM_001281806.1 | 2288 | Missense Mutation | TCT,TTT | S,F 657 | NP_001268735.1 | |
XM_005272425.4 | 2288 | Missense Mutation | TCT,TTT | S,F 702 | XP_005272482.1 | |
XM_011521235.2 | 2288 | Missense Mutation | TCT,TTT | S,F 625 | XP_011519537.1 | |
XM_017021924.1 | 2288 | Intron | XP_016877413.1 |
SCARNA15 - small Cajal body-specific RNA 15 | ||||||
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There are no transcripts associated with this gene. |
SNHG21 - small nucleolar RNA host gene 21 | ||||||
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There are no transcripts associated with this gene. |