Product Details
- SNP ID
-
rs190969738
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:37126931 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTCAACCTTGTGGGATGTGAAAACT[C/T]TGTTACTGAAGGTTAGTATCATATT
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZCCHC7
PubMed Links
Gene Details
- Gene
- ZCCHC7
- Gene Name
- zinc finger CCHC-type containing 7
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001289119.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
NP_001276048.1 |
NM_001289120.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
NP_001276049.1 |
NM_001289121.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
NP_001276050.1 |
NM_032226.2 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
NP_115602.2 |
XM_005251608.4 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
XP_005251665.1 |
XM_005251612.2 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
XP_005251669.1 |
XM_011518050.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
XP_011516352.1 |
XM_011518051.2 |
772 |
Intron |
|
|
XP_011516353.1 |
XM_017015197.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
XP_016870686.1 |
XM_017015198.1 |
772 |
Missense Mutation |
TCT,TTT |
S200F |
XP_016870687.1 |
XM_017015199.1 |
772 |
Missense Mutation |
CTG,TTG |
L17L |
XP_016870688.1 |
XM_017015200.1 |
772 |
Silent Mutation |
CTG,TTG |
L17L |
XP_016870689.1 |
XM_017015201.1 |
772 |
Intron |
|
|
XP_016870690.1 |
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