Product Details
- SNP ID
-
rs151219989
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:49697384 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCCTCAGTTGGCTTTTCCTCTTCA[A/G]TGCCATCCAGCTTGCCTGGTTCCTC
- Phenotype
-
MIM: 608846
MIM: 602950
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ADM5
PubMed Links
Gene Details
- Gene
- ADM5
- Gene Name
- adrenomedullin 5 (putative)
There are no transcripts associated with this gene.
- Gene
- CPT1C
- Gene Name
- carnitine palmitoyltransferase 1C
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001136052.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
NP_001129524.1 |
NM_001199752.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
NP_001186681.1 |
NM_001199753.1 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
NP_001186682.1 |
NM_152359.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
NP_689572.1 |
XM_005258505.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_005258562.1 |
XM_005258506.4 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_005258563.1 |
XM_006723009.3 |
609 |
UTR 5 |
|
|
XP_006723072.1 |
XM_011526438.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_011524740.1 |
XM_011526439.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_011524741.1 |
XM_011526440.2 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_011524742.1 |
XM_017026265.1 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_016881754.1 |
XM_017026266.1 |
609 |
Missense Mutation |
AAT,AGT |
N67S |
XP_016881755.1 |
XM_017026267.1 |
609 |
UTR 5 |
|
|
XP_016881756.1 |
XM_017026268.1 |
609 |
UTR 5 |
|
|
XP_016881757.1 |
XM_017026269.1 |
609 |
UTR 5 |
|
|
XP_016881758.1 |
XM_017026270.1 |
609 |
UTR 5 |
|
|
XP_016881759.1 |
XM_017026271.1 |
609 |
UTR 5 |
|
|
XP_016881760.1 |
XM_017026272.1 |
609 |
UTR 5 |
|
|
XP_016881761.1 |
XM_017026273.1 |
609 |
UTR 5 |
|
|
XP_016881762.1 |
- Gene
- PRMT1
- Gene Name
- protein arginine methyltransferase 1
There are no transcripts associated with this gene.
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