Product Details
- SNP ID
-
rs189519380
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
4
- Location
-
Chr.1:24651443 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGATCTCCTTCCCCTAGAAGACGA[C/T]CTTCCCCTGTCAGGAGAGAGAGAAA
- Phenotype
-
MIM: 605975
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SRRM1
PubMed Links
Gene Details
- Gene
- SRRM1
- Gene Name
- serine and arginine repetitive matrix 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001303448.1 |
2651 |
Missense Mutation |
CCT,TCT |
P186S |
NP_001290377.1 |
NM_001303449.1 |
2651 |
Intron |
|
|
NP_001290378.1 |
NM_005839.3 |
2651 |
Missense Mutation |
CCT,TCT |
P186S |
NP_005830.2 |
XM_005245717.2 |
2651 |
Intron |
|
|
XP_005245774.1 |
XM_005245718.2 |
2651 |
Intron |
|
|
XP_005245775.1 |
XM_005245720.2 |
2651 |
Intron |
|
|
XP_005245777.1 |
XM_005245721.2 |
2651 |
Intron |
|
|
XP_005245778.1 |
XM_005245722.2 |
2651 |
Intron |
|
|
XP_005245779.1 |
XM_011540478.2 |
2651 |
Intron |
|
|
XP_011538780.1 |
XM_011540479.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_011538781.1 |
XM_011540480.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_011538782.1 |
XM_011540481.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_011538783.1 |
XM_011540482.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_011538784.1 |
XM_011540483.1 |
2651 |
Intron |
|
|
XP_011538785.1 |
XM_017000011.1 |
2651 |
Intron |
|
|
XP_016855500.1 |
XM_017000012.1 |
2651 |
Intron |
|
|
XP_016855501.1 |
XM_017000013.1 |
2651 |
Intron |
|
|
XP_016855502.1 |
XM_017000014.1 |
2651 |
Intron |
|
|
XP_016855503.1 |
XM_017000015.1 |
2651 |
Intron |
|
|
XP_016855504.1 |
XM_017000016.1 |
2651 |
Intron |
|
|
XP_016855505.1 |
XM_017000017.1 |
2651 |
Intron |
|
|
XP_016855506.1 |
XM_017000018.1 |
2651 |
Intron |
|
|
XP_016855507.1 |
XM_017000019.1 |
2651 |
Intron |
|
|
XP_016855508.1 |
XM_017000020.1 |
2651 |
Intron |
|
|
XP_016855509.1 |
XM_017000021.1 |
2651 |
Intron |
|
|
XP_016855510.1 |
XM_017000022.1 |
2651 |
Intron |
|
|
XP_016855511.1 |
XM_017000023.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_016855512.1 |
XM_017000024.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_016855513.1 |
XM_017000025.1 |
2651 |
Intron |
|
|
XP_016855514.1 |
XM_017000026.1 |
2651 |
Intron |
|
|
XP_016855515.1 |
XM_017000027.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_016855516.1 |
XM_017000028.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_016855517.1 |
XM_017000029.1 |
2651 |
Missense Mutation |
CCT,TCT |
P103S |
XP_016855518.1 |
XM_017000030.1 |
2651 |
Intron |
|
|
XP_016855519.1 |
XM_017000031.1 |
2651 |
Intron |
|
|
XP_016855520.1 |
XM_017000032.1 |
2651 |
Intron |
|
|
XP_016855521.1 |
XM_017000033.1 |
2651 |
Intron |
|
|
XP_016855522.1 |
XM_017000034.1 |
2651 |
Intron |
|
|
XP_016855523.1 |
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