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H-Invitational ID: HIT000053157 Accession number: BC047523 Created date: 26-Mar-2013 Last modified: 27-May-2015
Definition: Calmodulin; CaM;
 
 

Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information  VaryGene Repeat mask viewer
 Single Nucleotide Polymorphism (SNP) and indel  VaryGene
Location Variation dbSNP ID Strand CDS/UTR Translation
30 .. 30 C/T rs188359112 + 5'UTR
35 .. 35 C/T rs146545930 + 5'UTR
39 .. 39 A/T rs181001910 + 5'UTR
42 .. 42 C/T rs141007341 + 5'UTR
51 .. 51 G/T rs12886186 + 5'UTR
117 .. 117 A/G rs12886342 + 5'UTR
171 .. 171 C/T rs12886083 + 5'UTR
271 .. 271 T/C rs144339242 + CDS Synonymous[Asp23Asp]
274 .. 274 C/T rs267607278 + CDS Synonymous[Gly24Gly]
321 .. 321 T/C rs199950662 + CDS Nonsynonymous[Leu40Pro]
327 .. 327 A/T rs199897752 + CDS Nonsynonymous[Gln42Leu]
351 .. 351 A/G rs202194260 + CDS Nonsynonymous[Gln50Arg]
363 .. 363 A/T rs267607276 + CDS Nonsynonymous[Asn54Ile]
445 .. 445 T/C rs200250055 + CDS Synonymous[Asp81Asp]
474 .. 474 G/A rs11541171 + CDS Nonsynonymous[Arg91Gln]
495 .. 495 A/G rs267607277 + CDS Nonsynonymous[Asn98Ser]
505 .. 505 C/T rs143503733 + CDS Synonymous[Ile101Ile]
526 .. 526 C/T rs139706811 + CDS Synonymous[His108His]
604 .. 604 C/T rs193072150 + CDS Synonymous[Asp134Asp]
628 .. 628 C/T rs199744595 + CDS Synonymous[Phe142Phe]
663 .. 663 T/G rs201339726 + 3'UTR
670 .. 670 C/T rs200742588 + 3'UTR
786 .. 786 T/C rs5871 + 3'UTR
890 .. 890 C/T rs112958092 + 3'UTR
990 .. 990 G/A rs187714594 + 3'UTR
1105 .. 1105 C/T rs1059285 + 3'UTR
1143 ^ 1144 -/GG rs139060064 + 3'UTR
1148 .. 1148 A/G rs199697317 - 3'UTR
1221 ^ 1222 -/T rs35149335 + 3'UTR
1224 .. 1224 T/- rs71771679 + 3'UTR
1224 ^ 1225 -/T rs71823341 + 3'UTR
1238 ^ 1239 -/T rs199855088 + 3'UTR
1238 ^ 1239 -/T/TTT rs56856377 + 3'UTR
1239 .. 1239 C/G/T rs111860684 + 3'UTR
1407 .. 1407 G/T rs11541170 - 3'UTR
1408 .. 1408 C/T rs116646015 + 3'UTR
1452 .. 1452 A/G rs1059296 + 3'UTR
1542 .. 1542 G/A rs61989066 + 3'UTR
1544 .. 1544 A/G rs77928599 + 3'UTR
1553 .. 1553 A/C/T rs77916091 + 3'UTR
1556 .. 1556 C/A rs78459823 + 3'UTR
1566 .. 1566 C/A rs146008731 + 3'UTR
1651 .. 1651 A/G rs115723958 + 3'UTR
1673 .. 1673 T/A rs138659409 + 3'UTR
1719 .. 1719 C/A rs75951656 + 3'UTR
1739 .. 1739 C/T rs192521929 + 3'UTR
1759 .. 1759 G/A rs183678923 + 3'UTR
1789 .. 1789 T/G rs3814846 - 3'UTR
1796 .. 1796 C/T rs61989067 + 3'UTR
1798 .. 1798 T/- rs71461907 + 3'UTR
1798 ^ 1799 -/C rs200711428 + 3'UTR
1799 .. 1799 T/C rs75202062 + 3'UTR
1813 .. 1813 C/G rs3814845 - 3'UTR
2050 .. 2050 A/G rs141870617 + 3'UTR
2066 .. 2066 G/A rs3814844 - 3'UTR
2210 .. 2210 C/T rs186848664 + 3'UTR
2238 .. 2238 C/T rs35418035 + 3'UTR
2320 .. 2320 T/G rs3814843 - 3'UTR
2332 .. 2332 C/A rs139692985 + 3'UTR
2384 .. 2384 G/A rs192452102 + 3'UTR
2453 .. 2453 A/G rs184803743 + 3'UTR
2494 .. 2494 T/C rs149760583 + 3'UTR
2571 .. 2571 A/G rs189778902 + 3'UTR
2579 .. 2579 T/C rs181805019 + 3'UTR
2586 .. 2586 G/T rs184371119 + 3'UTR
2618 .. 2618 T/G rs189147924 + 3'UTR
2619 .. 2619 T/C rs181955035 + 3'UTR
2719 .. 2719 G/C rs3179089 + 3'UTR
3021 .. 3021 C/T rs184950622 + 3'UTR
3080 .. 3080 C/A rs11539544 + 3'UTR
3105 .. 3105 C/T rs1058903 + 3'UTR
3315 .. 3315 C/G rs140025082 + 3'UTR
3348 .. 3348 C/T rs115172487 + 3'UTR
3456 .. 3456 A/G rs145426711 + 3'UTR
3586 .. 3586 G/A rs147728175 + 3'UTR
3645 .. 3645 G/C rs142500788 + 3'UTR
3651 .. 3651 T/C rs144946670 + 3'UTR
 Microsatellite (Short Tandem Repeat, STR)
No data available
 Microsatellite: Human-Gene diversity Of Life-style related Diseases (H-GOLD)
No data available
Mini-G

 Repeat  Repeat mask viewer
No data available
Database links H-GOLDHuman-Gene diversity Of Life-style related Diseases(H-GOLD)
Related H-InvDB links VaryGeneVaryGene;  Repeat mask viewerRepeat Mask Viewer